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Mr Phaco

FDA UDI

Class I (US FDA UDI)

by Crestpoint Management Ltd.

Identity

Trade Name
MR PHACO FDA UDI
Generic Name
Ophthalmic surgical device handling forceps, reusable FDA UDI
Device Name
Girard Tying Forceps Straight, Extra Delicate Straight Smooth Jaws with 5mm Tying Platform Round Knurled Handle with Guide Pin, 110mm Overall Length, Stainless Steel FDA UDI
Model / Reference
PH2279 FDA UDI
Description
Girard Tying Forceps Straight, Extra Delicate Straight Smooth Jaws with 5mm Tying Platform Round Knurled Handle with Guide Pin, 110mm Overall Length, Stainless Steel FDA UDI

Identifiers

Primary DI / UDI-DI
G412PH22790 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
Sterilization Method
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

Similar devices

Also classified as Ophthalmic surgical device handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Crestpoint Management Ltd.

Sources (1)

  • FDA UDI 5e35df95-bff6-4cea-bb20-5be40d0cd972 33 fields · synced Jun 8, 2026