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Citec

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 06975238201977Model DH-BF-232300CS

by Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd.

Identity

Trade Name
Biopsy Forcep EUDAMED
CITEC FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
Biopsy Forcep EUDAMED
Disposable Biopsy Forceps, 2.3*2300mm, Alligator Cup with Spike FDA UDI
Model / Reference
DH-BF-232300CS EUDAMED
06975238201977 EUDAMED
DH-BE-232300CS FDA UDI
Description
Disposable Biopsy Forceps, 2.3*2300mm, Alligator Cup with Spike FDA UDI

Identifiers

Primary DI / UDI-DI
06975238201977 EUDAMEDFDA UDI
Basic UDI-DI
B-06975238201977 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
Greece EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Citec by Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI eb67ca96-b099-4b26-9e72-0b82ece2d992 33 fields · synced Jul 9, 2026
  • EUDAMED 5314fded-4aae-41ee-a579-8a24cfeb2427 61 fields · synced Jul 9, 2026