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Novo Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical Inc. FDA UDI
Generic Name
Surgical clip rack FDA UDI
Device Name
michel suture clips, package of 1000, 11.0 mm FDA UDI
Model / Reference
G2491-22 FDA UDI
Description
michel suture clips, package of 1000, 11.0 mm FDA UDI

Identifiers

Catalog Number
G2491-22 FDA UDI
Primary DI / UDI-DI
00842331160783 FDA UDI
FDA Product Code
FZQ FDA UDI
GMDN Term
Surgical clip rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Surgical clip rack

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

Similar devices

Also classified as Surgical clip rack.

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 c1b7dbf8-541b-4f68-8410-9a83f00807c4 35 fields · synced May 30, 2026