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D-Kat T-Type (disposable Prism)
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 2414-P-2031Ref 2414-P-2032
by Keeler Ltd
Identity
- Trade Name
- D-KAT T-TYPE (DISPOSABLE PRISM) EUDAMEDFDA UDID-KAT (T-TYPE) EUDAMEDD-KAT T-Type FDA UDI
- Generic Name
- Ophthalmic tonometer, battery-operated FDA UDI
- Device Name
- D-KAT T-TYPE (DISPOSABLE PRISM) EUDAMEDD-KAT (T-TYPE) EUDAMED
- Model / Reference
- 2414-P-2031 EUDAMEDFDA UDI2414-P-2032 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055272716895 EUDAMEDFDA UDI05055272712200 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05055272716895 EUDAMEDB-05055272712200 EUDAMED
- FDA Product Code
- HKY FDA UDI
- EMDN Code
- Z12120122 TONOMETERS EUDAMED
- GMDN Term
- Ophthalmic tonometer, battery-operated FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 886.1930 FDA UDI
- Market of Registration
- Czechia EUDAMEDFinland 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
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
D-Kat T-Type (disposable Prism) by Keeler Ltd — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05055272716895 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Keeler Ltd
- EUDAMED SRN
- GB-MF-000009031
- Authorised Representative
- Keeler Europe Distribution, S.L. ES-AR-000001559
Sources (4)
- EUDAMED 60227bf4-5308-4631-9b4a-bb72624fde17 61 fields · synced Jul 15, 2026
- FDA UDI e835420d-6df1-48dc-948f-90d3c9e80899 32 fields · synced May 30, 2026
- FDA UDI 0290ca15-5762-49db-a0ea-5a936f654afc 32 fields · synced May 30, 2026
- EUDAMED cb5653ff-0ef9-4a8a-8794-9efb66e5dc21 61 fields · synced Jul 15, 2026