← Back to catalogue
Deflector Shaft, reusable
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref JSBDS3222
by Joimax GmbH
Identity
- Trade Name
- Deflector Shaft, reusable EUDAMEDdeflector schaft FDA UDI
- Generic Name
- Arthroscopic shaver system, electrically-powered FDA UDI
- Device Name
- Deflector Shaft, reusable EUDAMEDFDA UDI
- Model / Reference
- JSBDS3222 EUDAMEDFDA UDI
- Description
- Deflector Shaft, reusable FDA UDI
Identifiers
- Catalog Number
- JSBDS3222 FDA UDI
- Primary DI / UDI-DI
- 04250337103998 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337103998 EUDAMED
- FDA Product Code
- HWE FDA UDI
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Arthroscopic shaver system, electrically-powered FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4820 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
Deflector Shaft, reusable by Joimax GmbH — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04250337103998 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (2)
- EUDAMED 35058031-3c88-4757-8bc3-163117364a9c 61 fields · synced Jun 18, 2026
- FDA UDI b524fd6d-9492-45d4-8013-77370bd7ff58 36 fields · synced May 30, 2026