Mr Phaco

FDA UDI

Class I (US FDA UDI)

by Crestpoint Management Ltd.

Identity

Trade Name: MR PHACO FDA UDI
Generic Name: General-purpose surgical spatula FDA UDI
Device Name: Machat LASIK Retreatment Spatula DBL-Ended, Cylindrical Spatula with Slightly Pointed tip, Angled 8mm from bend to tip, / .8mm Wide Spatula, Flat Interior Edge with Rounded front tip, Angled 1.2mm from bend to tip, Round Knurled Handle, 120mm Overall Length, Titanium FDA UDI
Model / Reference: PH6572T FDA UDI
Description: Machat LASIK Retreatment Spatula DBL-Ended, Cylindrical Spatula with Slightly Pointed tip, Angled 8mm from bend to tip, / .8mm Wide Spatula, Flat Interior Edge with Rounded front tip, Angled 1.2mm from bend to tip, Round Knurled Handle, 120mm Overall Length, Titanium FDA UDI

Identifiers

Primary DI / UDI-DI: G412PH6572T0 FDA UDI
FDA Product Code: HND FDA UDI
GMDN Term: General-purpose surgical spatula 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical spatula

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 a71ccb8d-b005-47eb-ac2e-4da0ba3ed411 33 fields · synced Jun 8, 2026