Identity
- Trade Name
- TRYTABLE FDA UDI
- Generic Name
- General examination/treatment chair, electric FDA UDI
- Device Name
- TRYTABLE EUDAMEDThe TU2000 TRYTABLE is a medical device intended for use during examinations and minor surgical procedures in urological, urodynamic, gynaecological and similar examinations carried out in medical examination rooms in order to stabilise and position the patient. FDA UDI
- Model / Reference
- TU2000 EUDAMEDFDA UDI
- Description
- The TU2000 TRYTABLE is a medical device intended for use during examinations and minor surgical procedures in urological, urodynamic, gynaecological and similar examinations carried out in medical examination rooms in order to stabilise and position the patient. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08594211570411 EUDAMEDFDA UDI
- Basic UDI-DI
- 859421157TRYTABLES2 EUDAMED
- Direct Marketing DI
- 08594211570411 EUDAMED
- FDA Product Code
- MMZ FDA UDI
- EMDN Code
- V08020199 ELECTRIC MEDICAL CHAIRS - OTHER EUDAMED
- GMDN Term
- General examination/treatment chair, electric FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.4890 FDA UDI
- Market of Registration
- Czechia 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
No
FDA UDI
Trytable by MEDKONSULT medical technology s.r.o. — 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 | 859421157TRYTABLES2 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- MEDKONSULT medical technology s.r.o.
- EUDAMED SRN
- CZ-MF-000016193
Sources (2)
- EUDAMED 0e23b8b9-d9ec-4466-974e-840b4f2ceb78 61 fields · synced Jul 9, 2026
- FDA UDI a55b1986-473b-4ba4-948d-0f6dbfde980a 33 fields · synced May 30, 2026