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Spoongrasper Forceps

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JGF244590Ref JGF154570

by Joimax GmbH

Identity

Trade Name
Spoongrasper Forceps EUDAMED
Forceps FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
Spoongrasper Forceps EUDAMEDFDA UDI
Biopsy Forceps, Blakesley EUDAMED
Model / Reference
JGF244590 EUDAMEDFDA UDI
JGF154570 EUDAMEDFDA UDI
Description
Spoongrasper Forceps FDA UDI

Identifiers

Catalog Number
JGF154570 FDA UDI
JGF244590 FDA UDI
Primary DI / UDI-DI
04250337111856 EUDAMEDFDA UDI
04250337120438 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337111856 EUDAMED
42503371FORCGRAG8 EUDAMED
Direct Marketing DI
04250337120438 EUDAMED
FDA Product Code
GEN FDA UDI
EMDN Code
L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
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

Spoongrasper Forceps 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 (5)

  • EUDAMED 1adc1abe-e47b-49fc-8dea-8e5403081f5b 61 fields · synced Jul 10, 2026
  • EUDAMED b0d9a59a-0c0a-4be1-a0ff-bbdaadef89f2 61 fields · synced May 19, 2026
  • FDA UDI 17b6f988-37bf-4667-959f-94c9bff0ad15 36 fields · synced May 27, 2026
  • FDA UDI 6809d1e5-a860-4235-a36f-2755cca91c8f 36 fields · synced May 30, 2026
  • EUDAMED 4346691f-6105-45ae-8957-9272edbd3762 61 fields · synced Jul 10, 2026