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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
Instrument tray, reusable FDA UDI
Device Name
Microsurgical Plastic Instrument Sterilization Tray, 2.5"W x 6" L x .75" H deep base lid and silicone finger mat, accommodates 2-4 instruments FDA UDI
Model / Reference
T70031 FDA UDI
Description
Microsurgical Plastic Instrument Sterilization Tray, 2.5"W x 6" L x .75" H deep base lid and silicone finger mat, accommodates 2-4 instruments FDA UDI

Identifiers

Primary DI / UDI-DI
G412T700310 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Instrument tray, reusable

Mr Phaco by Crestpoint Management Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2e9eebd-72b2-4ace-adc7-b4d43f8285bf 33 fields · synced Jun 6, 2026