To: | CrossBay Medical, Inc. (trademark@lbhip.com) |
Subject: | U.S. Trademark Application Serial No. 88547107 - CROSSGLIDE - CRSSTZ00100 |
Sent: | October 22, 2019 01:51:12 PM |
Sent As: | ecom116@uspto.gov |
Attachments: |
United States Patent and Trademark Office (USPTO)
Office Action (Official Letter) About Applicant’s Trademark Application
U.S. Application Serial No. 88547107
Mark: CROSSGLIDE
|
|
Correspondence Address:
|
|
Applicant: CrossBay Medical, Inc.
|
|
Reference/Docket No. CRSSTZ00100
Correspondence Email Address: |
|
The USPTO must receive applicant’s response to this letter within six months of the issue date below or the application will be abandoned. Respond using the Trademark Electronic Application System (TEAS). A link to the appropriate TEAS response form appears at the end of this Office action.
Issue date: October 22, 2019
The referenced application has been reviewed by the assigned trademark examining attorney. Applicant must respond timely and completely to the issue(s) below. 15 U.S.C. §1062(b); 37 C.F.R. §§2.62(a), 2.65(a); TMEP §§711, 718.03.
Search Results
The trademark examining attorney has searched the Office’s database of registered and pending marks and has found no conflicting marks that would bar registration under Trademark Act Section 2(d). TMEP §704.02; see 15 U.S.C. §1052(d).
Identification of Goods
The identification of goods is indefinite and must be clarified because the nature of some of the items is unclear as noted below. The phrase “medical devices for access of devices, instruments, or cannula…” is indefinite because it is unclear whether this refers to devices that permit users to access and manipulate other devices that will be inserted into body cavities, or if it refers to the actual devices that are inserted and used for the delivery and removal of fluids and tissue samples.
The wording “catheters incontinence devices and access for devices for incontinence” is unacceptably indefinite because it is unclear if it refers to one type of device or multiple items. The applicant must amend this wording to specify the item(s) by common commercial name. See 37 C.F.R. §2.32(a)(6); TMEP §1402.01.
Applicant may adopt the following identification, if accurate:
Class 3:
Incontinence wipes impregnated with cleansing preparations
Class 5:
Incontinence garments
Class 10:
medical devices for use in treating and diagnosing [specify disease or condition device used for, e.g. diabetes, cancer, epilepsy, etc.]; medical instruments and cannula for insertion into bodily orifices, cavities, and lumena; medical instruments and cannula for insertion into potential spaces within a body; medical devices for use in the field of women's health, namely, medical instruments and catheters for use in gynecological procedures and gynecological surgical procedures; medical kits consisting primarily of medical instruments, catheters, and preparations for diagnosis and treatment of women's health issues; gynecological medical instruments; urological medical instruments for males and females; medical and surgical catheters; catheters and parts and fittings thereof; endoscopic equipment for medical purposes; hysteroscopes; cytoscopes; medical endoscopes; rigid and flexible medical endoscopes; medical devices used to evaluate the uterine cavity and patency of fallopian tubes; medical devices used to evaluate the bladder and urinary function; medical gynecological instruments for examining women's reproductive organs; medical urological instruments for examining the urinary tract function within males and females; nebulizers for medical purposes; medical fluid injectors; catheters for use in biopsies; fallopian tube biopsy instruments; uterine biopsy instruments; biopsy devices, namely, [specify items by common commercial name, e.g. scalpels, tissue samplers, tissue forceps, etc.]; biopsy instruments; medical instruments for use in performing biopsies; catheters for use in fallopian tube biopsies; catheters for use in uterine biopsies; medical instruments for uterine cell sampling; medical instrument for fallopian cell sampling; endometrial samplers; cytology brushes; endometrium biopsy suction devices; uterine access devices, namely, dilators and cannulae; incontinence devices, namely, [specify by common commercial name, e.g. bed pads, medical instruments for use in strengthening pelvic floor muscles, etc.]; uterine introducing catheters; balloon catheters; medical balloons; everting medical balloons; everting catheters; everting cervical catheters; medical devices for placing and securing catheters; inflation devices for balloon catheters; catheters for use in uterine access; catheters for use in fallopian tube access; medical balloons for use in cervical transit; medical instruments for stabilization of cervix; medical devices, namely, insemination catheters for delivering reproductive material to the uterus or fallopian tube; embryo transfer catheters and syringes; intra-uterine contraceptive devices; intra-uterine contraceptive device delivery instruments; medical instruments for the transfer of sperm and semen; medical instruments for egg transfer; medical and surgical dilators; vaginal dilators; cervical dilators, bodily lumen or vessel dilators; dilators for potential spaces within a male or female body; uterine dilators
Classification
Combined Application Requirements
(1) List the goods and/or services by their international class number in consecutive numerical order, starting with the lowest numbered class.
(2) Submit a filing fee for each international class not covered by the fee(s) already paid (view the USPTO’s current fee schedule). The application identifies goods and/or services that are classified in at least 3 classes; however, applicant submitted a fee(s) sufficient for only 1 class. Applicant must either submit the filing fees for the classes not covered by the submitted fees or restrict the application to the number of classes covered by the fees already paid.
See 15 U.S.C. §§1051(b), 1112, 1126(e); 37 C.F.R. §§2.32(a)(6)-(7), 2.34(a)(2)-(3), 2.86(a); TMEP §§1403.01, 1403.02(c).
See an overview of the requirements for a Section 1(b) multiple-class application and how to satisfy the requirements online using the Trademark Electronic Application System (TEAS) form.
TEAS PLUS OR TEAS REDUCED FEE (TEAS RF) APPLICANTS – TO MAINTAIN LOWER FEE, ADDITIONAL REQUIREMENTS MUST BE MET, INCLUDING SUBMITTING DOCUMENTS ONLINE: Applicants who filed their application online using the lower-fee TEAS Plus or TEAS RF application form must (1) file certain documents online using TEAS, including responses to Office actions (see TMEP §§819.02(b), 820.02(b) for a complete list of these documents); (2) maintain a valid e-mail correspondence address; and (3) agree to receive correspondence from the USPTO by e-mail throughout the prosecution of the application. See 37 C.F.R. §§2.22(b), 2.23(b); TMEP §§819, 820. TEAS Plus or TEAS RF applicants who do not meet these requirements must submit an additional processing fee of $125 per class of goods and/or services. 37 C.F.R. §§2.6(a)(1)(v), 2.22(c), 2.23(c); TMEP §§819.04, 820.04. However, in certain situations, TEAS Plus or TEAS RF applicants may respond to an Office action by authorizing an examiner’s amendment by telephone or e-mail without incurring this additional fee.
How to respond. Click to file a response to this nonfinal Office action
/Karen Bracey/
Examining Attorney
Law Office 116
571-272-9132
karen.bracey@uspto.gov
RESPONSE GUIDANCE