Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Surgical FDA UDI
Generic Name: Corneoscleral punch FDA UDI
Device Name: Gass corneoscleral punch, 3 1/2'', 1.5mm diameter head, 0.75mm bite, rotatable tip FDA UDI
Model / Reference: Gass corneoscleral punch FDA UDI
Description: Gass corneoscleral punch, 3 1/2'', 1.5mm diameter head, 0.75mm bite, rotatable tip FDA UDI

Identifiers

Catalog Number: 9102E FDA UDI
Primary DI / UDI-DI: 00190660128234 FDA UDI
FDA Product Code: HNJ FDA UDI
GMDN Term: Corneoscleral punch 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Corneoscleral punch

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

Similar devices

Also classified as Corneoscleral punch.

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Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
V. Mueller — STERIS CORPORATION · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ambler Surgical, LLC

Sources (1)

FDA UDI fd35cde7-54a3-420c-938e-391f9098efa3 35 fields · synced May 30, 2026