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iLESSYS® Pro Guiding Rod, conical, blunt, green
EUDAMEDFDA UDIClass I (EU MDR)
Ref GRC260024
by Joimax GmbH
Identity
- Trade Name
- iLESSYS® Pro Guiding Rod, conical, blunt, green EUDAMEDiLESSYS® FDA UDI
- Generic Name
- Endoscopic-access dilator, reusable FDA UDI
- Device Name
- iLESSYS® Pro Guiding Rod, conical, blunt, green EUDAMEDFDA UDIGuiding Tube, Rod EUDAMED
- Model / Reference
- GRC260024 EUDAMEDFDA UDI
- Description
- iLESSYS® Pro Guiding Rod, conical, blunt, green FDA UDI
Identifiers
- Catalog Number
- GRC260024 FDA UDI
- Primary DI / UDI-DI
- 04250337115861 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337115861 EUDAMED42503371DILADIL9L 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
iLESSYS® Pro Guiding Rod, conical, blunt, green 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-04250337115861 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-04250337115861 | 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 fcc90435-461d-450d-869a-bc32cbf29799 61 fields · synced Jun 19, 2026
- EUDAMED c401d663-bd45-4393-ba72-5af3b1327d19 61 fields · synced May 19, 2026
- FDA UDI e48ea6ee-d804-4945-8c8c-0a3f23e5448d 36 fields · synced May 30, 2026