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PROGRESSIVE-LINE Tap
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref J5071.3800
by ALTATEC GmbH
Identity
- Trade Name
- PROGRESSIVE-LINE Tap EUDAMEDTap PROGRESSIVE-LINE FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- Tap PROGRESSIVE-LINE EUDAMEDTap PROGRESSIVE-LINE, d 3.8 mm FDA UDI
- Model / Reference
- J5071.3800 EUDAMEDFDA UDI
- Description
- Tap PROGRESSIVE-LINE, d 3.8 mm FDA UDI
Identifiers
- Catalog Number
- J5071.3800 FDA UDI
- Primary DI / UDI-DI
- 04099797995428 EUDAMEDE219J507138001 FDA UDI
- Basic UDI-DI
- 40997970004031000000000EX EUDAMED
- Secondary DI
- E219J507138001 EUDAMED
- FDA Product Code
- EJL FDA UDI
- EMDN Code
- Z12110102 DENTAL DRILLS EUDAMED
- GMDN Term
- Bone tap, 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 — 3.8 Millimeter FDA UDI
PROGRESSIVE-LINE Tap 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 | 40997970004031000000000EX | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 106ff196-8b89-4e37-aeb6-a4eb662888f1 61 fields · synced Jul 30, 2026
- FDA UDI 814e8b4a-fe01-4187-b5ac-303b27cfe4ba 36 fields · synced May 29, 2026