← Back to catalogue

Cage Pusher Head concave

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JCPH221021C

by Joimax GmbH

Identity

Trade Name
Cage Pusher Head concave EUDAMED
joimax® Cage Pusher Head concave EUDAMED
Look-up tool FDA UDI
Generic Name
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
Cage Pusher Head concave EUDAMEDFDA UDI
joimax® Cage Pusher EUDAMED
Model / Reference
JCPH221021C EUDAMEDFDA UDI
Description
Cage Pusher Head concave FDA UDI

Identifiers

Catalog Number
JCPH221021C FDA UDI
Primary DI / UDI-DI
04250337114857 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337114857 EUDAMED
42503371INCAPUSEM EUDAMED
Direct Marketing DI
04250337114857 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical implant/trial-implant/sizer holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Class IIa EUDAMED
Regulation Number
888.4540 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

EUDAMEDEUDAMED

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

Cage Pusher Head concave by Joimax GmbH — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED 868f880c-0afa-48f2-97ab-8710be580622 61 fields · synced Jul 20, 2026
  • FDA UDI b3f8ff32-8f30-4110-b7c0-ea3fae6e3642 36 fields · synced May 29, 2026
  • EUDAMED 70b8505b-aca0-49b7-9cb9-51c94371e3f4 61 fields · synced Jul 20, 2026