Deflector Diamond Abrasor, disposable
EUDAMEDFDA UDIClass IIa (EU MDR)
by Joimax GmbH
Identity
- Trade Name
- Deflector Diamond Abrasor, disposable EUDAMEDDeflector Diamond Abrasor EUDAMEDdeflector FDA UDI
- Generic Name
- Arthroscopic shaver system blade, single-use FDA UDI
- Device Name
- Deflector Diamond Abrasor, disposable EUDAMEDFDA UDIDeflector Diamond Abrasor EUDAMEDFDA UDI
- Model / Reference
- JSBDD3115 EUDAMEDFDA UDIJSBDD3235 EUDAMEDFDA UDI
- Description
- Deflector Diamond Abrasor, disposable FDA UDIDeflector Diamond Abrasor FDA UDI
Identifiers
- Catalog Number
- JSBDD3115 FDA UDIJSBDD3235 FDA UDI
- Primary DI / UDI-DI
- 04250337118701 EUDAMEDFDA UDI04250337103264 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337118701 EUDAMEDB-04250337103264 EUDAMED42503371DEFLABR7K EUDAMED42503371DEFLCUT9S EUDAMED
- Direct Marketing DI
- 04250337118701 EUDAMED04250337103264 EUDAMED
- FDA Product Code
- HWE FDA UDI
- EMDN Code
- Z12130585 MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- Arthroscopic shaver system blade, single-use 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
Yes
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Spinal shaver system blade
Deflector Diamond Abrasor, disposable by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal shaver system blade.
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
CE/MDD
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-04250337118701 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-04250337118701 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (6)
- EUDAMED 993c0386-116a-4bba-ac69-45d8f5371403 61 fields · synced Jul 23, 2026
- EUDAMED acc5c36e-a40d-415e-ab80-e37010d4e336 61 fields · synced May 17, 2026
- FDA UDI de577ac6-5c93-480a-b473-595d88147ea4 36 fields · synced May 30, 2026
- FDA UDI 4194d79f-d431-4285-8aa6-28b9e6b13d45 36 fields · synced May 30, 2026
- EUDAMED c58b4f51-20c6-42b9-8a9a-76907d83aa1d 61 fields · synced Jun 18, 2026
- EUDAMED 3484e3e4-b331-4dd5-a05a-ecd30f6c086e 61 fields · synced Jul 9, 2026