← Back to catalogue
Photographic Mirror Crystal for Occlusal L
EUDAMEDFDA UDIClass I (EU MDR)
Ref 13282Model DENTAL MIRRORS
Identity
- Trade Name
- Photographic Mirror Crystal for Occlusal L EUDAMEDNA FDA UDI
- Generic Name
- Dental mirror, reusable FDA UDI
- Device Name
- Photographic Mirror EUDAMEDUsed to assist practitioners during general surgery by displaying the image of an object placed before it. FDA UDI
- Model / Reference
- DENTAL MIRRORS EUDAMED13282 EUDAMEDFDA UDI
- Description
- Used to assist practitioners during general surgery by displaying the image of an object placed before it. FDA UDI
Identifiers
- Catalog Number
- 13282 FDA UDI
- Primary DI / UDI-DI
- 04963931132829 EUDAMEDFDA UDI
- Basic UDI-DI
- 4963931YDM00004WL EUDAMED
- FDA Product Code
- EAX FDA UDI
- EMDN Code
- L160201 DENTAL MIRRORS AND HANDLES, REUSABLE EUDAMED
- GMDN Term
- Dental mirror, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Spain 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Photographic Mirror Crystal for Occlusal L by Ydm Corporation — 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 | 4963931YDM00004WL | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ydm Corporation
- EUDAMED SRN
- JP-MF-000011653
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (2)
- EUDAMED 11a0470e-5926-405e-aedf-c276d53d417d 61 fields · synced Jul 8, 2026
- FDA UDI 393bf044-fddc-4355-94f1-e93cedf1c112 35 fields · synced May 30, 2026