Identity
- Trade Name
- Digitest™ EUDAMEDFDA UDI
- Generic Name
- Dental pulp analysis system FDA UDI
- Device Name
- Digitest 3 EUDAMEDDigitest™ 3 Pulp Vitality Tester EUDAMEDDigitest™ 3 Digital Pulptester FDA UDI
- Model / Reference
- D655 EUDAMEDFDA UDID655E EUDAMED
- Description
- Digitest™ 3 Digital Pulptester FDA UDI
Identifiers
- Catalog Number
- D655 FDA UDI
- Primary DI / UDI-DI
- 00810000520862 EUDAMEDFDA UDI00810000520688 EUDAMED
- Basic UDI-DI
- B-00810000520862 EUDAMEDB-00810000520688 EUDAMED
- FDA Product Code
- EAT FDA UDI
- EMDN Code
- Z12119005 PULP VITALITY ANALYSERS EUDAMED
- GMDN Term
- Dental pulp analysis system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 872.1720 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Digitest™ by Parkell, Inc. — 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-00810000520862 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Parkell Inc.
- EUDAMED SRN
- US-MF-000003761
- Authorised Representative
- Directa AB SE-AR-000002492
Sources (3)
- EUDAMED f61f7b12-c720-4e29-b783-73b86eb28caa 61 fields · synced Jul 16, 2026
- EUDAMED d9029c38-8bbd-47e6-b488-26e9b1bc99ef 61 fields · synced May 18, 2026
- FDA UDI 85ad5b0a-5bfd-456d-83ca-d906cb52ab66 36 fields · synced May 30, 2026