Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › Endomyocardial biopsy forceps, single-use
Device Explorer · FDA GUDID · GMDN 46679

Endomyocardial biopsy forceps, single-use

A sterile grasping instrument designed to obtain tissue samples from the inner walls of the heart (endomyocardium) typically for histopathological examination. It is typically a flexible metal coil or plastic tube with a pair of scissors-like cups with cutting

US‑registered devices85in commercial distribution
Companies11labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription95%Rx‑only share
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Share of device records

Atc Technologies, Inc.2226%
Argon Medical Devices, Inc.1619%
Fehling Instruments Gmbh & Co. Kg1012%
St. Jude Medical, Inc.78%
Scholten Surgical Instruments, Inc.78%
Cook Incorporated67%
Cordis Us Corp.56%
Merit Medical Systems, Inc.45%

Top labelers

CompanyDevicesShare
Atc Technologies, Inc.2226%
Argon Medical Devices, Inc.1619%
Fehling Instruments Gmbh & Co. Kg1012%
St. Jude Medical, Inc.78%
Scholten Surgical Instruments, Inc.78%
Cook Incorporated67%
Cordis Us Corp.56%
Merit Medical Systems, Inc.45%
Deroyal Industries, Inc.45%
Lake Region Medical22%
Cordis Corporation22%

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

Brand names on the register (sample)

Procure™NAJawz Endomyocardial Biopsy ForcepJawz Endomyocardial Biopsy ForcepsNovatome™NovatomeCookSparrowHawkultraCbxDeRoyalBIPALBIOPSY FORCEPS STDBiopsy Forceps

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

FDA product codes

CodeNameDevices
DWZDevice, Biopsy, Endomyocardial57
DWZDEVICE, BIOPSY, ENDOMYOCARDIAL21
LROGeneral surgery tray3
DWETUBING, PUMP, CARDIOPULMONARY BYPASS3
OFGCT biopsy tray1

GMDN & GCC registration

  • GMDN code 46679 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 95% · 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) · 9Catheter Gauge (French) · 7Outer Diameter (Femtometer) · 2

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

No closely related category with 50+ devices.

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

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

Which FDA product codes apply?

DWZ (Device, Biopsy, Endomyocardial), DWZ (DEVICE, BIOPSY, ENDOMYOCARDIAL), LRO (General surgery tray), DWE (TUBING, PUMP, CARDIOPULMONARY BYPASS)

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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