← Back to catalogue

Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Surgical flat-nosed pliers FDA UDI
Device Name
Narrow nose wire pulling forceps, 7 1/2'', serrated jaws, 3.0mm tips FDA UDI
Model / Reference
Narrow nose wire pulling forceps FDA UDI
Description
Narrow nose wire pulling forceps, 7 1/2'', serrated jaws, 3.0mm tips FDA UDI

Identifiers

Catalog Number
64-400 FDA UDI
Primary DI / UDI-DI
00190660126834 FDA UDI
FDA Product Code
HTC FDA UDI
GMDN Term
Surgical flat-nosed pliers 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

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: Surgical flat-nosed pliers

Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical flat-nosed pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e72a7bc5-e05e-47e0-8a25-5a3984a26a95 35 fields · synced May 30, 2026