← Back to catalogue

Guiding Tube, conical, violet

EUDAMEDFDA UDI

Class I (EU MDR)

Ref GTC151510

by Joimax GmbH

Identity

Trade Name
Guiding Tube, conical, violet EUDAMED
guiding sleeve FDA UDI
Generic Name
Endoscopic-access dilator, reusable FDA UDI
Device Name
Guiding Tube, conical, violet EUDAMEDFDA UDI
Guiding Tube, Rod EUDAMED
Model / Reference
GTC151510 EUDAMEDFDA UDI
Description
Guiding Tube, conical, violet FDA UDI

Identifiers

Catalog Number
GTC151510 FDA UDI
Primary DI / UDI-DI
04250337109259 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337109259 EUDAMED
42503371DILADIL9L EUDAMED
FDA Product Code
FZX FDA UDI
EMDN Code
L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Endoscopic-access dilator, 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

Guiding Tube, conical, violet 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 08672f76-949b-4c28-96fd-32b342164ee9 61 fields · synced Jul 24, 2026
  • EUDAMED fe2d6eb8-0696-4e66-8164-762258764022 61 fields · synced May 18, 2026
  • FDA UDI 120c9ca5-992f-43ea-adfe-a41656cf0140 36 fields · synced May 29, 2026