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Mp-2785-G23

FDA UDI

Class II (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name
MP-2785-G23 FDA UDI
Generic Name
Needle guide, reusable FDA UDI
Device Name
Needle Guide FDA UDI
Model / Reference
MP-2785-G23 FDA UDI
Description
Needle Guide FDA UDI

Identifiers

Primary DI / UDI-DI
04573596214312 FDA UDI
FDA Product Code
IYO FDA UDI
IYN FDA UDI
ITX FDA UDI
GMDN Term
Needle guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1550 FDA UDI
892.1570 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 23 Gauge FDA UDI

Category: Needle guide, reusable

Mp-2785-G23 by FUJIFILM Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FUJIFILM Corporation

Sources (1)

  • FDA UDI 82ce9656-7adc-4dca-9ce0-14ff07d5e61f 35 fields · synced May 30, 2026