Identity
- Trade Name
- PROGNOST XP EUDAMEDFDA UDI
- Generic Name
- Basic diagnostic x-ray system table, non-powered FDA UDI
- Device Name
- PROGNOST XP EUDAMEDBasic diagnostic x-ray system table, non-powered FDA UDI
- Model / Reference
- 7036-0-1714 EUDAMEDtable top 226x75,5cm carbon fiber FDA UDI
- Description
- Basic diagnostic x-ray system table, non-powered FDA UDI
Identifiers
- Catalog Number
- 7036-0-1714 FDA UDI
- Primary DI / UDI-DI
- 04260502640241 EUDAMEDFDA UDI
- Basic UDI-DI
- 426050264X009ZT EUDAMED
- FDA Product Code
- KXJ FDA UDI
- EMDN Code
- Z11030503 PATIENT TABLES FOR RADIOLOGICAL EQUIPMENT EUDAMED
- GMDN Term
- Basic diagnostic x-ray system table, non-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1980 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
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 — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Basic diagnostic x-ray system table, non-powered.
- SPT2 Radiographic Table — CARESTREAM HEALTH, INC. · Class II
- Large Veterinary Platform — Neurologica Corporation · Class II
- NEONATAL SCANNING PLATFORM, NL5000 — Neurologica Corporation · Class II
- PEDIATRIC SCANNING PLATFORM FOR OMNITOM — Neurologica Corporation · Class II
- SEDECAL — Sedecal., Sa. · Class II
- PATIENT TABLE — Pausch, L.L.C. · Class II
- CARESTREAM SPT1 Radiographic Table — CARESTREAM HEALTH, INC. · Class II
- Neo-Natal Scanning Platform — Neurologica Corporation · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- PROTEC GmbH & Co. KG
Sources (2)
- FDA UDI bca1a6bd-18f8-4ee1-9f6c-6ea19ee02826 35 fields · synced Jul 28, 2026
- EUDAMED a8338214-70eb-4620-adce-546308fa57e2 61 fields · synced Jul 28, 2026