quick clamping drilling attachment
FDA UDIEUDAMEDClass I (US FDA UDI)
by Joimax, Inc.
Identity
- Trade Name
- joimax® Drill Chuck, keyless, AO EUDAMEDquick clamping drilling attachment FDA UDI
- Generic Name
- Arthroscopic shaver system, electrically-powered FDA UDI
- Device Name
- joimax® Drill Chuck, keyless, AO EUDAMEDFDA UDI
- Model / Reference
- JSDCAO100 EUDAMEDFDA UDI
- Description
- joimax® Drill Chuck, keyless, AO FDA UDI
Identifiers
- Catalog Number
- JSDCAO100 FDA UDI
- Primary DI / UDI-DI
- 04250337112495 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371SHRIDRILLDR EUDAMED
- Direct Marketing DI
- 04250337112495 EUDAMED
- FDA Product Code
- HWE FDA UDI
- EMDN Code
- Z12130580 MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Arthroscopic shaver system, electrically-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
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
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
Yes
Category: Arthroscopic shaver system, electrically-powered
quick clamping drilling attachment by Joimax, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Arthroscopic shaver system, electrically-powered.
- Formula — Stryker Corp. · Class I
- Formula — Stryker Corp. · Class I
- Formula — Stryker Corp. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- FMS — Medos International Sàrl · Class II
- Arthrex® — Arthrex, Inc. · Class I
- Formula — Stryker Corp. · Class I
- Arthrex® — Arthrex, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Joimax, Inc.
Sources (2)
- FDA UDI b1c034ae-5a8e-4c5c-914b-42d044b8eb74 35 fields · synced Jul 9, 2026
- EUDAMED 5d7bbae7-74a2-446b-9082-2e7d31556a41 61 fields · synced Jul 9, 2026