Precisor

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 00821C

by Conmed Corporation

Identity

Trade Name: Precisor EUDAMEDFDA UDI
Generic Name: Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name: Non-orthopedic, Non-active, Instrument, Endoscopic, Biopsy Forceps EUDAMED
PRECISOR JUMBO COATED DISPOSABLE BIOPSY FORCEPS, OVAL CUP WITH NEEDLE, 3.10 MM X 230 CM FDA UDI
Model / Reference: 00821C EUDAMEDFDA UDI
Description: PRECISOR JUMBO COATED DISPOSABLE BIOPSY FORCEPS, OVAL CUP WITH NEEDLE, 3.10 MM X 230 CM FDA UDI

Identifiers

Catalog Number: 00821C FDA UDI
Primary DI / UDI-DI: 30653405052078 EUDAMEDFDA UDI
Basic UDI-DI: B-30653405052078 EUDAMED
FDA Product Code: FCL FDA UDI
EMDN Code: G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED
GMDN Term: Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class: Class IIa EUDAMED
Class I FDA UDI
Regulation Number: 876.1075 FDA UDI
Market of Registration: Belgium EUDAMED
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

EUDAMEDFDA UDI

Reusable

EUDAMED

Contains Latex

EUDAMEDFDA UDI

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Dimensions & Sizes

Size: Width — 3.1 Millimeter FDA UDI
Outer Diameter — 3.7 Millimeter FDA UDI
Length — 230 Centimeter FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Precisor by Conmed Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Disposable Biopsy Forceps — Yangzhou Fartley Medical Instrument Technology Co., Ltd. · Class IIa
Single Use Biopsy Forceps — Zhejiang Chuangxiang Medical Technology Co., LTD. · Class I
Disposable Endoscopic Biopsy Forceps — Ningbo Xinwell Medical Technology Co., Ltd. · Class I
POWER-ENDO — Jiangsu Power-endo Medical Technology Co., Ltd · Class IIa
Single Use Biopsy Forceps — ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD. · Class IIa
Single-use Biopsy Forceps — Anrei Medical (HZ) CO., LTD. · Class IIa
Disposable Biopsy Forceps — Jiangsu Ate Medical Technology Co., Ltd. · Class IIa
Disposable Biopsy Forceps — Endoaccess GmbH · Class IIa

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	CE/MDD	B-30653405052078	Class IIa	Active
FDA UDI	United States	FDA UDI	Registered in GUDID	Class IIa	Pending data

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Manufacturer

Manufacturer: Conmed Corporation
EUDAMED SRN: US-MF-000012663
Authorised Representative: MDSS GmbH DE-AR-000005430

Sources (2)

EUDAMED f60a657a-d89c-4b9f-9168-1fb3d15b2ddf 61 fields · synced May 30, 2026
FDA UDI 24162884-5651-4b16-a9f6-adad39c2cd70 36 fields · synced May 30, 2026