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Biopsy Forceps, steerable 35°, down-biting

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JSF3303520D

by Joimax GmbH

Identity

Trade Name
Biopsy Forceps, steerable 35°, down-biting EUDAMED
Forceps FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
Biopsy Forceps, steerable 35°, down-biting EUDAMEDFDA UDI
Biopsy Forceps EUDAMED
Model / Reference
JSF3303520D EUDAMEDFDA UDI
Description
Biopsy Forceps, steerable 35°, down-biting FDA UDI

Identifiers

Catalog Number
JSF3303520D FDA UDI
Primary DI / UDI-DI
04250337109525 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337109525 EUDAMED
42503371FORCFORGU 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

Biopsy Forceps, steerable 35°, down-biting 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 f3b1dbc7-bdb6-4fba-8de9-84e2c1acf6f5 61 fields · synced Jun 19, 2026
  • EUDAMED d19c1e03-981f-4462-8307-6a9ea3e58638 61 fields · synced May 18, 2026
  • FDA UDI 6cbd6fc3-9dfd-4746-8ff6-04143af02318 36 fields · synced May 30, 2026