Identity
- Trade Name
- Castroviejo Caliper (non glare), refurb. FDA UDI
- Generic Name
- Ophthalmic calliper FDA UDI
- Device Name
- The Caliper is a measuring instrument intended to measure the skin or the eyelids' muscles that the surgeon wants to remove or shorten. The instrument touches directly onto the patient's eyelid and tissue that will be operated. It is partially non-glare: the ruler is not surface treated. It is usually used before the laser. Full scale is 20 mm and resolution is 0.5 mm. FDA UDI
- Model / Reference
- 25-140R FDA UDI
- Description
- The Caliper is a measuring instrument intended to measure the skin or the eyelids' muscles that the surgeon wants to remove or shorten. The instrument touches directly onto the patient's eyelid and tissue that will be operated. It is partially non-glare: the ruler is not surface treated. It is usually used before the laser. Full scale is 20 mm and resolution is 0.5 mm. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10697660003525 FDA UDI
- FDA Product Code
- FTY FDA UDI
- GMDN Term
- Ophthalmic calliper FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Castroviejo Caliper (non glare), refurb. by Oculo-Plastik Inc — 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 |
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Manufacturer
- Manufacturer
- Oculo-Plastik Inc
Sources (1)
- FDA UDI a06c0292-48bf-4a45-bc46-b683f81b5c49 36 fields · synced May 31, 2026