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Keyes Vulvar Punch

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Keyes Vulvar Punch FDA UDI
Generic Name
Skin-coring punch, reusable FDA UDI
Device Name
Keyes Vulvar Punch (3 mm) FDA UDI
Model / Reference
68-173 FDA UDI
Description
Keyes Vulvar Punch (3 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00888937018349 FDA UDI
FDA Product Code
EME FDA UDI
GMDN Term
Skin-coring punch, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3 Millimeter FDA UDI

Category: Skin-coring punch, reusable

Keyes Vulvar Punch by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-coring punch, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d76baf39-1064-480b-98be-c02d5344e4d5 34 fields · synced Jun 9, 2026