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Multi Level BB Pronged Blade

FDA UDI

Class II (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
Multi Level BB Pronged Blade FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Multi Level Black Belt Pronged Blade 70mm Standard Width, Aluminum FDA UDI
Model / Reference
7325-73 FDA UDI
Description
Multi Level Black Belt Pronged Blade 70mm Standard Width, Aluminum FDA UDI

Identifiers

Catalog Number
7325-73 FDA UDI
Primary DI / UDI-DI
10840199513762 FDA UDI
FDA Product Code
GZT FDA UDI
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 FDA UDI
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 22 Millimeter FDA UDI
Depth — 70 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Multi Level BB Pronged Blade by Koros USA, Inc. — Class II — 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

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Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI ff073c7b-268c-4ada-988d-04efc7bc9d84 37 fields · synced Jun 6, 2026