Identity
- Trade Name
- MR PHACO FDA UDI
- Generic Name
- Ophthalmic surgical device handling forceps, reusable FDA UDI
- Device Name
- Utrata MICS Capsulorhexis Forceps Jaws set to open only 1.8mm from tip to bend, Angled 12mm from bend to tip with Extremely Thin Triangular Grasping Tips, Serrated Flat Handle, 80mm Overall Length, Stainless Steel FDA UDI
- Model / Reference
- PH1017-1 FDA UDI
- Description
- Utrata MICS Capsulorhexis Forceps Jaws set to open only 1.8mm from tip to bend, Angled 12mm from bend to tip with Extremely Thin Triangular Grasping Tips, Serrated Flat Handle, 80mm Overall Length, Stainless Steel FDA UDI
Identifiers
- Primary DI / UDI-DI
- G412PH101710 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic surgical device handling forceps, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic surgical device handling forceps, reusable
Mr Phaco by Crestpoint Management Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Crestpoint Management Ltd.
Sources (1)
- FDA UDI 55abea16-b6de-4318-b463-47686e683e18 33 fields · synced May 30, 2026