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Greenwald Surgical Company, Inc.

FDA UDI

Class I (US FDA UDI)

by Grace Manufacturing Inc

Identity

Trade Name
Greenwald Surgical Company, Inc. FDA UDI
Generic Name
Vessel retractor FDA UDI
Device Name
Stamey Dorsal Vein Apical Retractor. Stainless steel throughout. Handle flange provides secure control and cephaled retraction. Retractor blades provide a wide space on both sides of the dorsal vein complex for placing a controlling suture. FDA UDI
Model / Reference
51200-00 FDA UDI
Description
Stamey Dorsal Vein Apical Retractor. Stainless steel throughout. Handle flange provides secure control and cephaled retraction. Retractor blades provide a wide space on both sides of the dorsal vein complex for placing a controlling suture. FDA UDI

Identifiers

Catalog Number
U530 FDA UDI
Primary DI / UDI-DI
10801334011901 FDA UDI
FDA Product Code
FGN FDA UDI
GMDN Term
Vessel retractor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Category: Vessel retractor

Greenwald Surgical Company, Inc. by Grace Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Manufacturing Inc

Sources (1)

  • FDA UDI 130f579a-a389-41fd-8601-bf13804f2c68 34 fields · synced May 30, 2026