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Grasper Forceps, down-biting

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CGF232020D

by Joimax GmbH

Identity

Trade Name
Grasper Forceps, down-biting EUDAMED
Forceps FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
Biopsy Forceps, Blakesley EUDAMED
Grasper Forceps, down-biting EUDAMEDFDA UDI
Model / Reference
CGF232020D EUDAMEDFDA UDI
Description
Grasper Forceps, down-biting FDA UDI

Identifiers

Catalog Number
CGF232020D FDA UDI
Primary DI / UDI-DI
04250337100188 EUDAMEDFDA UDI
Basic UDI-DI
42503371FORCGRAG8 EUDAMED
B-04250337100188 EUDAMED
FDA Product Code
GEN FDA UDI
EMDN Code
L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
GMDN Term
Rigid endoscopic biopsy 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

Grasper Forceps, down-biting by Joimax GmbH — Class I — MDD, MDR, 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/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED ccdb87f6-cd0f-42ea-9696-dd4239074610 61 fields · synced Jul 30, 2026
  • EUDAMED 3defe2da-ebd2-40a7-99da-db1d5c81aa43 61 fields · synced May 17, 2026
  • FDA UDI c2081276-864c-4474-b18c-89c908c7a6ed 36 fields · synced May 30, 2026