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Symmetry Greenberg®

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Greenberg® FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Greenberg Retractor; Clamp; Secondary; 12 in; 305 mm FDA UDI
Model / Reference
50-1508 FDA UDI
Description
Greenberg Retractor; Clamp; Secondary; 12 in; 305 mm FDA UDI

Identifiers

Catalog Number
50-1508 FDA UDI
Primary DI / UDI-DI
00887482017272 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

Dimensions & Sizes

Size
Length — 12 Inch FDA UDI

Category: Surgical retraction system, reusable

Symmetry Greenberg® by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 513f03eb-e6e6-482e-8afc-7d3bd5104d6e 36 fields · synced May 30, 2026