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Halyard

FDA UDI

Class I (US FDA UDI)

by Avid Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Model / Reference
NLEB009_0002 FDA UDI

Identifiers

Catalog Number
NLEB009 FDA UDI
Primary DI / UDI-DI
10809160320488 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use

Halyard by Avid Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avid Medical, Inc.

Sources (1)

  • FDA UDI 0a1ef9c6-8537-49c2-95b4-f583c64942ab 34 fields · synced May 30, 2026