← Back to catalogue
Anschlusskabel-S Touchproof für Tubus-Klebeelektroden
EUDAMEDFDA UDIClass I (EU MDR)
Ref 530665Model 530663
Identity
- Trade Name
- Anschlusskabel-S Touchproof für Tubus-Klebeelektroden EUDAMEDN/A FDA UDI
- Generic Name
- Electromyographic endotracheal tube FDA UDI
- Device Name
- Anschlusskabel Touchproof für Tubus-Klebeelektroden EUDAMEDConnecting cable S shielded f. inomed laryngeal electrodesTouchproof FDA UDI
- Model / Reference
- 530663 EUDAMED530665 EUDAMEDFDA UDI
- Description
- Connecting cable S shielded f. inomed laryngeal electrodesTouchproof FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250307603381 EUDAMEDEINO5306659 FDA UDI
- Basic UDI-DI
- 42503076IZC0148K EUDAMED
- FDA Product Code
- ETN FDA UDI
- EMDN Code
- Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Electromyographic endotracheal tube FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 874.1820 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic trocar blade, reusable
Anschlusskabel-S Touchproof für Tubus-Klebeelektroden by inomed Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Similar devices
Also classified as Orthopaedic trocar blade, reusable.
- Trauma Fixation Systems — Biomet Orthopedics, Inc. · Class I
- LEVEL ONE TRANSBUCCAL — KLS-Martin L.P. · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
- EBA ONE — Citieffe · Class II
- ARTHROLUTION — Richard Wolf GmbH · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
- Arthrex® — Arthrex, Inc. · Class I
- R3 — Smith & Nephew, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 42503076IZC0148K | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- inomed Medizintechnik GmbH
- EUDAMED SRN
- DE-MF-000005589
Sources (2)
- EUDAMED 30246e96-4fa9-4f51-a358-f50c7e23e02a 61 fields · synced Jul 18, 2026
- FDA UDI cede6a4c-8327-4450-a03d-6967cfe8e6d3 34 fields · synced May 30, 2026