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Clamping Tube

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JMPS1052R

by Joimax GmbH

Identity

Trade Name
Clamping Tube EUDAMEDFDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Clamping Tube EUDAMEDFDA UDI
Model / Reference
JMPS1052R EUDAMEDFDA UDI
Description
Clamping Tube FDA UDI

Identifiers

Catalog Number
JMPS1052R FDA UDI
Primary DI / UDI-DI
04250337110545 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337110545 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Austria 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

Clamping Tube by Joimax GmbH — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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 (2)

  • EUDAMED 37cfe90f-3b6e-4c9e-b0e1-612811794da9 61 fields · synced Jun 18, 2026
  • FDA UDI 4a3e6cd5-d049-45d8-a0fa-bac4e4608dfe 35 fields · synced May 30, 2026