Sony

FDA UDI

Class I (US FDA UDI)

by Sony Corporation

Identity

Trade Name: SONY FDA UDI
Generic Name: Video printer FDA UDI
Device Name: COLOR VIDEO PRINTER FDA UDI
Model / Reference: UP-25MD FDA UDI
Description: COLOR VIDEO PRINTER FDA UDI

Identifiers

Primary DI / UDI-DI: 04548736111714 FDA UDI
FDA Product Code: KQM FDA UDI
GMDN Term: Video printer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4160 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Video printer

Sony by Sony Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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SONY UP-D711MD Black &White Printer(KP+) — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
B/W video printer(FDA) Kit — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
SONY UP-D711MD Black & White Printer — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
SONY — PENTAX of America, 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: Sony Corporation

Sources (1)

FDA UDI 6d48c95f-b514-4a84-b6ba-bee8572f3250 33 fields · synced Jun 8, 2026