Endoch

FDA UDI

Class I (US FDA UDI)

by Endoch Inc

Identity

Trade Name: Endoch FDA UDI
Generic Name: Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name: DISPOSABLE BIOPSY FORCEPS, WITHOUT SPIKE, NON-COATED FDA UDI
Model / Reference: DBF-2316AF FDA UDI
Description: DISPOSABLE BIOPSY FORCEPS, WITHOUT SPIKE, NON-COATED FDA UDI

Identifiers

Catalog Number: DBF-2316AF FDA UDI
Primary DI / UDI-DI: DBF231613 FDA UDI
FDA Product Code: HFB FDA UDI
FCL FDA UDI
GMDN Term: Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4530 FDA UDI
876.1075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Endoch by Endoch Inc — Class I — FDA UDI — listed in 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 (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Endoch Inc

Sources (1)

FDA UDI 5a24a05f-4035-489f-8324-c20c9154e940 34 fields · synced Jun 1, 2026