Identity
- Trade Name
- Easyloupe 2,5 x, Titan FDA UDI
- Generic Name
- Magnifying spectacles FDA UDI
- Device Name
- Easyloupe 2,5 x, Titan FDA UDI
- Model / Reference
- 39735 FDA UDI
- Description
- Easyloupe 2,5 x, Titan FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049584019417 FDA UDI
- FDA Product Code
- HOI FDA UDI
- GMDN Term
- Magnifying spectacles FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5840 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Easyloupe 2, 5 x, Titan by OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
Sources (1)
- FDA UDI 253a881e-db2e-41de-9b2b-0b132f65a576 35 fields · synced May 30, 2026