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Bone Perforator, Drill Tip
EUDAMEDFDA UDIClass I (EU MDR)
Ref JMSNT20
by Joimax GmbH
Identity
- Trade Name
- Bone Perforator, Drill Tip EUDAMEDbone perforator FDA UDI
- Generic Name
- Bone awl, reusable FDA UDI
- Device Name
- Bone Drill EUDAMEDBone Perforator, Drill Tip EUDAMEDFDA UDI
- Model / Reference
- JMSNT20 EUDAMEDFDA UDI
- Description
- Bone Perforator, Drill Tip FDA UDI
Identifiers
- Catalog Number
- JMSNT20 FDA UDI
- Primary DI / UDI-DI
- 04250337110651 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371REAMDRIEW EUDAMEDB-04250337110651 EUDAMED
- FDA Product Code
- HTO FDA UDI
- EMDN Code
- L1113 NEUROSURGERY BURS AND TIPS, REUSABLE EUDAMED
- GMDN Term
- Bone awl, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 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
Bone Perforator, Drill Tip by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 42503371REAMDRIEW | Class I | Active |
| EUDAMED | European Union | CE/MDR | 42503371REAMDRIEW | 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 ab5ac39b-f339-4bd6-998b-f85a2a98e227 61 fields · synced Jul 14, 2026
- EUDAMED 4879e5df-162a-4e8c-9d5f-7f667a2bfa08 61 fields · synced May 17, 2026
- FDA UDI cd66e926-365e-4000-a439-6a4c79a43d9e 36 fields · synced May 30, 2026