← Back to catalogue
joimax® Arthroscope Combo
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AS4070175Ref AS4045175
by Joimax GmbH
Identity
- Trade Name
- joimax® Arthroscope Combo EUDAMEDjoimax® FDA UDI
- Generic Name
- Rigid optical arthroscope, reusable FDA UDI
- Device Name
- joimax® Arthroscope Combo EUDAMEDjoimax® Arthroscope Combo WL 175 mm / OD 4.0 mm / 70° FDA UDIjoimax® Arthroscope Combo WL 175 mm / OD 4.0 mm / 45° FDA UDI
- Model / Reference
- AS4070175 EUDAMEDFDA UDIAS4045175 EUDAMEDFDA UDI
- Description
- joimax® Arthroscope Combo WL 175 mm / OD 4.0 mm / 70° FDA UDIjoimax® Arthroscope Combo WL 175 mm / OD 4.0 mm / 45° FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250337100041 EUDAMEDFDA UDI04250337100034 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337100041 EUDAMEDB-04250337100034 EUDAMED42503371ENSCARTFV EUDAMED
- Direct Marketing DI
- 04250337100041 EUDAMED04250337100034 EUDAMED
- 510(k) Number
- K051827 FDA UDI
- FDA Product Code
- HRX FDA UDI
- EMDN Code
- Z12021101 ARTHROSCOPES EUDAMED
- GMDN Term
- Rigid optical arthroscope, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Market of Registration
- Germany EUDAMEDTürkiye 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
EUDAMEDEUDAMED
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
joimax® Arthroscope Combo by Joimax GmbH — Class IIa — 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-04250337100041 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-04250337100041 | 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 (6)
- EUDAMED 71e7f6cb-4708-4485-aa30-60c888689e9e 61 fields · synced Jul 23, 2026
- EUDAMED c7feedaa-8076-40e0-b9c0-b80b7fd370a9 61 fields · synced May 17, 2026
- FDA UDI 4260cd60-f36d-4baa-81f5-feb11fe1e377 35 fields · synced May 30, 2026
- FDA UDI b8a2e09f-a46d-4774-803e-e03286801657 35 fields · synced May 30, 2026
- EUDAMED 1d01b760-d47f-4368-8ffe-c039b3fa78ef 61 fields · synced Jul 8, 2026
- EUDAMED 49940898-7e7e-40f2-abe5-e815fd2591fd 61 fields · synced Jul 23, 2026