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PROGRESSIVE-LINE Surgery tray
EUDAMEDFDA UDIClass I (EU MDR)
Ref J5300.8920
by ALTATEC GmbH
Identity
- Trade Name
- PROGRESSIVE-LINE Surgery tray EUDAMEDSurgery-Tray PROGRESSIVE-LINE Flex FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- Surgery Tray PROGRESSIVE-LINE Flex EUDAMEDSurgery-Tray PROGRESSIVE-LINE Flex FDA UDI
- Model / Reference
- J5300.8920 EUDAMEDFDA UDI
- Description
- Surgery-Tray PROGRESSIVE-LINE Flex FDA UDI
Identifiers
- Catalog Number
- J5300.8920 FDA UDI
- Primary DI / UDI-DI
- 04099797012798 EUDAMEDE219J530089201 FDA UDI
- Basic UDI-DI
- 40997970008202000000000LD EUDAMED
- Secondary DI
- E219J530089201 EUDAMED
- FDA Product Code
- FSM FDA UDI
- EMDN Code
- Z12110180 INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
PROGRESSIVE-LINE Surgery tray by ALTATEC GmbH — Class I — 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 | 40997970008202000000000LD | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 9f2c8344-a9b8-4555-a773-ef33607f57df 61 fields · synced May 31, 2026
- FDA UDI 24855bed-705c-40d9-a31c-0a3f2de58680 35 fields · synced May 30, 2026