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Semi-flexible Crocodile Forceps, curved

EUDAMEDFDA UDI

Class I (EU MDR)

Ref TFC322755

by Joimax GmbH

Identity

Trade Name
Semi-flexible Crocodile Forceps, curved EUDAMED
Forceps FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Semi-flexible Crocodile Forceps, curved EUDAMEDFDA UDI
Semi-Flexible Grasper Forceps EUDAMED
Model / Reference
TFC322755 EUDAMEDFDA UDI
Description
Semi-flexible Crocodile Forceps, curved FDA UDI

Identifiers

Catalog Number
TFC322755 FDA UDI
Primary DI / UDI-DI
04250337109921 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337109921 EUDAMED
42503371FORCSEMHM EUDAMED
FDA Product Code
GEN FDA UDI
EMDN Code
L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Flexible endoscopic biopsy forceps, reusable

Semi-flexible Crocodile Forceps, curved by Joimax GmbH — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED 59debbff-6454-4cab-8919-6a872b445074 61 fields · synced Jul 25, 2026
  • EUDAMED e79899e7-a659-4dbd-9240-157ea7f06b64 61 fields · synced May 19, 2026
  • FDA UDI aa3bf884-7a28-47a0-a5fa-d9274544ebb5 36 fields · synced May 29, 2026