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Novo Surgical

FDA UDI

Class II (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical FDA UDI
Generic Name
Surgical A/V-shaped microvessel clamp FDA UDI
Device Name
Cooley Partial Occlusion Clamp, jaws 2.3 cm deep, 7.0 mm wide, 7-3/4" (19.5 cm) FDA UDI
Model / Reference
C6672-46 FDA UDI
Description
Cooley Partial Occlusion Clamp, jaws 2.3 cm deep, 7.0 mm wide, 7-3/4" (19.5 cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00842331124556 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical A/V-shaped microvessel clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

Dimensions & Sizes

Size
Length — 19.5 Centimeter FDA UDI

Category: Surgical A/V-shaped microvessel clamp

Novo Surgical by Novo Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical A/V-shaped microvessel clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novo Surgical, Inc.

Sources (1)

  • FDA UDI fe572f3c-cc6b-4824-a415-709b1ea0e903 34 fields · synced Jun 1, 2026