Clifford Offset Blade Retractor

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name: Clifford Offset Blade Retractor FDA UDI
Generic Name: Hand-held surgical retractor, reusable FDA UDI
Device Name: Clifford Offset Blade Retractor 22cm 18mm width FDA UDI
Model / Reference: 7236-40 FDA UDI
Description: Clifford Offset Blade Retractor 22cm 18mm width FDA UDI

Identifiers

Catalog Number: 7236-40 FDA UDI
Primary DI / UDI-DI: 10840199508621 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Hand-held surgical retractor, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held surgical retractor, reusable

Clifford Offset Blade Retractor by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Koros USA, Inc.

Sources (1)

FDA UDI d96891fe-0434-478d-b314-79b674d3b0ef 37 fields · synced May 30, 2026