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CESSYS® Dorsal Guiding Tube, beveled 45°, edged, yllw
EUDAMEDFDA UDIClass I (EU MDR)
Ref GRC142549
by Joimax GmbH
Identity
- Trade Name
- CESSYS® Dorsal Guiding Tube,beveled 45°,edged,yllw EUDAMEDCESSYS® FDA UDI
- Generic Name
- Endoscopic-access dilator, reusable FDA UDI
- Device Name
- Guiding Tube, Rod EUDAMEDCESSYS® Dorsal Guiding Tube,beveled 45°,edged,yllw EUDAMEDFDA UDI
- Model / Reference
- GRC142549 EUDAMEDFDA UDI
- Description
- CESSYS® Dorsal Guiding Tube,beveled 45°,edged,yllw FDA UDI
Identifiers
- Catalog Number
- GRC142549 FDA UDI
- Primary DI / UDI-DI
- 04250337116882 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371DILADIL9L EUDAMEDB-04250337116882 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
Moist Heat or Steam Sterilization FDA UDI
CESSYS® Dorsal Guiding Tube, beveled 45°, edged, yllw by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 42503371DILADIL9L | Class I | Active |
| EUDAMED | European Union | CE/MDR | 42503371DILADIL9L | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (3)
- EUDAMED 7b7b9cdb-28bb-48df-8c3e-0991d1dd0b7f 61 fields · synced Jul 30, 2026
- EUDAMED 6c808c4a-85f2-4826-b170-60d38196b19b 61 fields · synced May 17, 2026
- FDA UDI 69a97175-dd4b-4dae-8be3-e4d44ad59d4f 36 fields · synced May 30, 2026