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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
Needle guard FDA UDI
Device Name
flat caps, gas or steam permeable, can be used in flash or conventional autoclave processes, latex-free, 100 per package, 3/8" x 1" x 2mm, clear FDA UDI
Model / Reference
9122-01 FDA UDI
Description
flat caps, gas or steam permeable, can be used in flash or conventional autoclave processes, latex-free, 100 per package, 3/8" x 1" x 2mm, clear FDA UDI

Identifiers

Catalog Number
9122-01 FDA UDI
Primary DI / UDI-DI
00842331189920 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Needle guard FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Needle guard

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

Similar devices

Also classified as Needle guard.

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 99448608-d3d2-4688-88cb-e991328f8084 35 fields · synced Jun 1, 2026