← Back to catalogue

Ambler Surgical

FDA UDI

Class II (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Intestinal forceps FDA UDI
Device Name
DeBakey vascular tissue forceps, 8", standard, bayonet, 2.0mm tapered atraumatic tips, flat handle FDA UDI
Model / Reference
29-155 FDA UDI
Description
DeBakey vascular tissue forceps, 8", standard, bayonet, 2.0mm tapered atraumatic tips, flat handle FDA UDI

Identifiers

Catalog Number
29-155 FDA UDI
Primary DI / UDI-DI
00190660050252 FDA UDI
510(k) Number
K092544 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Intestinal forceps FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

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: Intestinal forceps

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

Similar devices

Also classified as Intestinal forceps.

Cleared under the same submission

K092544 also covers:

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

Manufacturer
Ambler Surgical, LLC

Sources (1)

  • FDA UDI fc435283-180c-4a05-9655-e181a7204cfd 36 fields · synced Jun 8, 2026