Identity
- Trade Name
- PROGNOST XP FDA UDI
- Generic Name
- Basic diagnostic x-ray system table, non-powered FDA UDI
- Device Name
- Basic diagnostic x-ray system table, non-powered FDA UDI
- Model / Reference
- table top 200x75,5cm composite fiber FDA UDI
- Description
- Basic diagnostic x-ray system table, non-powered FDA UDI
Identifiers
- Catalog Number
- 7036-0-1711 FDA UDI
- Primary DI / UDI-DI
- 04260502640210 FDA UDI
- FDA Product Code
- KXJ FDA UDI
- GMDN Term
- Basic diagnostic x-ray system table, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Basic diagnostic x-ray system table, non-powered
Prognost Xp by PROTEC GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- PROTEC GmbH & Co. KG
Sources (1)
- FDA UDI a344e83e-475a-414b-98fd-ecda8f0bda21 35 fields · synced Jun 8, 2026