Device Explorer · FDA GUDID · GMDN 34951

Bulldog clamp

A manual surgical instrument with heavily serrated jaws at the working end designed to grasp, join, compress or support an organ, vessel or tissue. This instrument is typically made of high-grade stainless steel and comes in two main designs: 1) a flat, pincer

US‑registered devices113in commercial distribution
Companies3labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Ambler Surgical Corp.10896%
Novo Surgical, Inc.33%
Scanlan International Inc22%

Top labelers

CompanyDevicesShare
Ambler Surgical Corp.10896%
Novo Surgical, Inc.33%
Scanlan International Inc22%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

SCANLAN®Novo SurgicalAmbler Surgical

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
DXCCLAMP, VASCULAR111
GDJClamp, Surgical, General & Plastic Surgery2

GMDN & GCC registration

  • GMDN code 34951 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 3

Use these as the dimensions to specify in a tender line.

How many bulldog clamp products are registered in the US?

113 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bulldog clamp", from 3 companies. The largest labeler is Ambler Surgical Corp. with 96% of records.

Which FDA product codes apply?

DXC (CLAMP, VASCULAR), GDJ (Clamp, Surgical, General & Plastic Surgery)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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