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Device Explorer · FDA GUDID · GMDN 61481

Open-surgery biopsy forceps, single-use

A hand-held manual surgical instrument designed to obtain soft-tissue biopsy specimens from an open surgical wound or from within/near a large natural orifice (e.g., vagina, rectum) for histopathological examination; it is not intended for endoscopic or cathet

US‑registered devices76in commercial distribution
Companies11labelers on GUDID
Single‑use92%of device records
Sterile89%labelled sterile
Prescription46%Rx‑only share
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Share of device records

Robbins Instruments Inc.2026%
Marina Medical Instruments, Inc.1722%
Dtr Medical Limited1114%
Owens & Minor Distribution, Inc.912%
Henry Schein, Inc.912%
Robinson Healthcare Limited45%
Churahi Surgical Co.23%
Zhejiang Chuangxiang Medical Technology Co., Ltd.11%

Top labelers

CompanyDevicesShare
Robbins Instruments Inc.2026%
Marina Medical Instruments, Inc.1722%
Dtr Medical Limited1114%
Owens & Minor Distribution, Inc.912%
Henry Schein, Inc.912%
Robinson Healthcare Limited45%
Churahi Surgical Co.23%
Zhejiang Chuangxiang Medical Technology Co., Ltd.11%
Bailey Instruments Ltd11%
Zinnanti Surgical Design Group Inc11%
Elmed Instruments(Pvt)Ltd.11%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Single Use Biopsy ForcepsSusol® Henckel Tilley Punch Forceps 4.5mmOral Biopsy Punch Long 180 mmOral Rotating Biopsy Punch 120 mmCervical Rotating Biopsy Punch SAMPLE SETOral Biopsy Forceps Long 180 mmOral Rotating Biopsy Forceps 120 mmCervical Biopsy PunchBaby Tischler Cervical Biopsy PunchTischler Cervical Biopsy PunchOral Biopsy Forceps Long 120mmOral Biopsy Forceps 90mmInstrapacMarina MedicalRobbins True-Cut Disposable Biopsy PunchesHalyard

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

FDA product codes

CodeNameDevices
LRYPUNCH, SURGICAL55
HFBForceps, Biopsy, Gynecological7
EMEPunch, Biopsy, Surgical6
HFBFORCEPS, BIOPSY, GYNECOLOGICAL4
NWWHysteroscope Accessories1
KAEForceps, Ent1

GMDN & GCC registration

  • GMDN code 61481 · non‑implantable
  • Single‑use 92% · sterile 89% · Rx‑only 46% · 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 (Millimeter) · 11Length (Centimeter) · 4

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

How many open-surgery biopsy forceps, single-use products are registered in the US?

76 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Open-surgery biopsy forceps, single-use", from 11 companies. The largest labeler is Robbins Instruments Inc. with 26% of records.

Which FDA product codes apply?

LRY (PUNCH, SURGICAL), HFB (Forceps, Biopsy, Gynecological), EME (Punch, Biopsy, Surgical), HFB (FORCEPS, BIOPSY, GYNECOLOGICAL)

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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