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Novo Surgical

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical FDA UDI
Generic Name
Eyelid clamp, reusable FDA UDI
Device Name
mueller/putterman-type (ptosis lid clamp) muscle forceps and clamp, 3 3/4", concave 22.0mm jaws with 6 pins FDA UDI
Model / Reference
NS5-9315 FDA UDI
Description
mueller/putterman-type (ptosis lid clamp) muscle forceps and clamp, 3 3/4", concave 22.0mm jaws with 6 pins FDA UDI

Identifiers

Primary DI / UDI-DI
G586NS593150 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Eyelid clamp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Eyelid clamp, reusable

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

Similar devices

Also classified as Eyelid clamp, reusable.

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 6d96f0cf-aaa9-4708-b32f-f12bef1a4a81 33 fields · synced Jun 6, 2026