← Back to catalogue
PROGRESSIVE-LINE Dense bone drill 2
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref J5072.4302
by ALTATEC GmbH
Identity
- Trade Name
- PROGRESSIVE-LINE Dense bone drill 2 EUDAMEDDense bone drill 2 PROGRESSIVE-LINE FDA UDI
- Generic Name
- Fixture/appliance dental drill bit, reusable FDA UDI
- Device Name
- Dense bone drill (2) PROGRESSIVE-LINE EUDAMEDDense bone drill 2 PROGRESSIVE-LINE, d 4.3 mm FDA UDI
- Model / Reference
- J5072.4302 EUDAMEDFDA UDI
- Description
- Dense bone drill 2 PROGRESSIVE-LINE, d 4.3 mm FDA UDI
Identifiers
- Catalog Number
- J5072.4302 FDA UDI
- Primary DI / UDI-DI
- 04099797995473 EUDAMEDE219J507243021 FDA UDI
- Basic UDI-DI
- 40997970004032000000000FU EUDAMED
- Secondary DI
- E219J507243021 EUDAMED
- FDA Product Code
- EJL FDA UDI
- EMDN Code
- Z12110102 DENTAL DRILLS EUDAMED
- GMDN Term
- Fixture/appliance dental drill bit, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.3240 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
No
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
Dimensions & Sizes
- Size
- Outer Diameter — 4.3 Millimeter FDA UDI
PROGRESSIVE-LINE Dense bone drill 2 by ALTATEC GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 40997970004032000000000FU | 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
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 90a1d444-bb9a-4819-a958-ffa0ed7b3abe 61 fields · synced May 31, 2026
- FDA UDI fab19b58-411d-4c52-b210-19fe008e68ce 36 fields · synced May 30, 2026