← Back to catalogue

Cosgrove Valve Retractor System

FDA UDI

Class I (US FDA UDI)

by Kapp Surgical Instrument, Inc.

Identity

Trade Name
Cosgrove Valve Retractor System FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Tricuspid Retractor Blade (custom 8" handle length) FDA UDI
Model / Reference
KS-7101-8 FDA UDI
Description
Tricuspid Retractor Blade (custom 8" handle length) FDA UDI

Identifiers

Catalog Number
KS-7101-8 FDA UDI
Primary DI / UDI-DI
B033KS71018 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Cosgrove Valve Retractor System by Kapp Surgical Instrument, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 838cbd8d-1b50-453f-b567-b1b61fae14b0 35 fields · synced Jun 9, 2026