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GelPOINT V-Path

FDA UDI

Class II (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name
GelPOINT V-Path FDA UDI
Generic Name
Radial surgical retractor seal cap FDA UDI
Device Name
Transvaginal Access Platform with Total vNOTES Access System FDA UDI
Model / Reference
C2C15 FDA UDI
Description
Transvaginal Access Platform with Total vNOTES Access System FDA UDI

Identifiers

Primary DI / UDI-DI
10607915145368 FDA UDI
FDA Product Code
MOK FDA UDI
GMDN Term
Radial surgical retractor seal cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radial surgical retractor seal cap

GelPOINT V-Path by Applied Medical Resources Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radial surgical retractor seal cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Medical Resources Corp.

Sources (1)

  • FDA UDI e04ea0c5-0a9e-46e2-a237-5dba2069e7f8 35 fields · synced May 30, 2026