Identity
- Trade Name
- PRO3DURE GR-1guide FDA UDI
- Generic Name
- Earmould, custom-made FDA UDI
- Device Name
- printodent GR-1 guide FDA UDI
- Model / Reference
- 1kg - clear-transparent FDA UDI
- Description
- printodent GR-1 guide FDA UDI
Identifiers
- Primary DI / UDI-DI
- EPRCD1000300 FDA UDI
- FDA Product Code
- DYT FDA UDI
- GMDN Term
- Earmould, custom-made FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.5525 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Earmould, custom-madeRemovable dental occlusal splint, custom-made
PRO3DURE GR-1guide by Pro3Dure Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Removable dental occlusal splint, custom-made.
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- Vertex-Dental BV — Vertex-Dental B.V. · Class I
- M-PM Crystal — Merz Dental GmbH · U
- M-PM Crystal — Merz Dental GmbH · U
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 I | Pending data |
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Manufacturer
- Manufacturer
- Pro3Dure Medical
Sources (1)
- FDA UDI 44f5146c-7c64-472f-b39f-3bf1c9e43010 35 fields · synced May 29, 2026