Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Surgical FDA UDI
Generic Name: Surgical penis clamp, reusable FDA UDI
Device Name: Vascular forceps, 5 1/4'', fully curved, serrated jaws, ring handle FDA UDI
Model / Reference: Vascular forceps FDA UDI
Description: Vascular forceps, 5 1/4'', fully curved, serrated jaws, ring handle FDA UDI

Identifiers

Catalog Number: 34-119 FDA UDI
Primary DI / UDI-DI: 00190660076801 FDA UDI
FDA Product Code: DWS FDA UDI
GMDN Term: Surgical penis clamp, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.4500 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: Surgical penis clamp, reusable

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

Similar devices

Also classified as Surgical penis clamp, reusable.

GEN2 — SURGIX MEDICAL LLC · Class I
American Medicals — AMERICAN MEDICALS · Class I
STOCKMANN PENIS FORCEPS — SONTEC INSTRUMENTS, INC. · Class I
Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
AESCULAP — AESCULAP, INC. · Class II
No-Scalpel Vasectomy — Femcare , Ltd. · Class I
AESCULAP — AESCULAP, INC. · Class II

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

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

Manufacturer

Manufacturer: Ambler Surgical, LLC

Sources (1)

FDA UDI 1b270673-0236-4ce4-a991-e7f693fe1d13 35 fields · synced Jun 1, 2026