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Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, reusable FDA UDI
Device Name
Bainbridge intestinal forceps, 6 1/8'', extra delicate, straight, longitudinal serrated jaws, ring handle FDA UDI
Model / Reference
Bainbridge intestinal forceps FDA UDI
Description
Bainbridge intestinal forceps, 6 1/8'', extra delicate, straight, longitudinal serrated jaws, ring handle FDA UDI

Identifiers

Catalog Number
26-377 FDA UDI
Primary DI / UDI-DI
00190660040550 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, 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

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: Dressing/utility forceps, scissors-like, reusable

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

Similar devices

Also classified as Dressing/utility forceps, scissors-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambler Surgical, LLC

Sources (1)

  • FDA UDI 91d59a70-01f3-4822-90c8-9fae7b9a9f6b 35 fields · synced Jun 6, 2026