Identity
- Trade Name
- MR PHACO FDA UDI
- Generic Name
- Ophthalmic surgical device handling forceps, reusable FDA UDI
- Device Name
- Sheets-McPherson Tying Forceps with 1mm of tips is crisscross serrated, Angled 45 Degree at 10.5mm from bend to tip, with 10mm Tying Platform, Serrated Flat Handle, 82mm Overall Length, Stainless Steel FDA UDI
- Model / Reference
- PH2258 FDA UDI
- Description
- Sheets-McPherson Tying Forceps with 1mm of tips is crisscross serrated, Angled 45 Degree at 10.5mm from bend to tip, with 10mm Tying Platform, Serrated Flat Handle, 82mm Overall Length, Stainless Steel FDA UDI
Identifiers
- Primary DI / UDI-DI
- G412PH22580 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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- gSource — GSOURCE, LLC. · Class I
- Walcott Rx Products — Walcott Rx Product Inc · Class I
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 39b5e821-2907-477c-b6fc-1440909e01c3 33 fields · synced May 30, 2026