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Titanium Chalazion Curette Double Ended, 2.5mm and 3.5mm
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Titanium Chalazion Curette Double Ended, 2.5mm and 3.5mm FDA UDI
- Generic Name
- Ophthalmic curette, reusable FDA UDI
- Model / Reference
- 1700-2535D FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840096200171 FDA UDI
- FDA Product Code
- FZS FDA UDI
- GMDN Term
- Ophthalmic curette, reusable 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
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
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
Titanium Chalazion Curette Double Ended, 2.5mm and 3.5mm by Katalyst Surgical, Llc — 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
- Katalyst Surgical, Llc
Sources (1)
- FDA UDI a0c9a696-59e3-458a-a281-33f0ac08d80e 33 fields · synced May 30, 2026