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Barraquer Needle Holder, Curved

FDA UDI

Class I (US FDA UDI)

by Bausch & Lomb, Inc.

Identity

Trade Name
Barraquer Needle Holder, Curved FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Model / Reference
E3828 CW FDA UDI

Identifiers

Primary DI / UDI-DI
04058935011581 FDA UDI
FDA Product Code
HNM FDA UDI
GMDN Term
Suturing needle holder, 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing needle holder, reusable

Barraquer Needle Holder, Curved by Bausch & Lomb, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bausch & Lomb, Inc.

Sources (1)

  • FDA UDI 556adbf0-1fbf-4914-9f04-a678311369a8 32 fields · synced Jun 8, 2026