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Guide Wire with markers, straight, non-sterile

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JPGW38015

by Joimax GmbH

Identity

Trade Name
Guide Wire with markers, straight, non-sterile EUDAMED
guide wire FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
Guide Wire with markers, straight, non-sterile EUDAMEDFDA UDI
Guide Wire with marker, straight, non-sterile EUDAMED
Model / Reference
JPGW38015 EUDAMEDFDA UDI
Description
Guide Wire with markers, straight, non-sterile FDA UDI

Identifiers

Catalog Number
JPGW38015 FDA UDI
Primary DI / UDI-DI
04250337114239 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337114239 EUDAMED
42503371GUWIGUWPV EUDAMED
Direct Marketing DI
04250337114239 EUDAMED
FDA Product Code
FZX FDA UDI
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Class IIa EUDAMED
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

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

Guide Wire with markers, straight, non-sterile 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

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED fe4e4aac-7ba0-4db3-ac34-94f3669d1d18 61 fields · synced Jun 18, 2026
  • FDA UDI fda419ec-d6c0-4526-9a72-211819b926e8 36 fields · synced May 30, 2026
  • EUDAMED 5fac8e84-b245-4d31-ae57-3687a49ae60f 61 fields · synced Jun 18, 2026