Eview

FDA UDI

Class II (US FDA UDI)

by Zhuhai Pusen Medical Technology Co, Ltd

Identity

Trade Name: Eview FDA UDI
Generic Name: Endoscopic video image processing unit FDA UDI
Device Name: This equipment has been designed to be used to process signals from an endoscope and convert it to a signal that can be displayed on the monitor. FDA UDI
Model / Reference: PV210 FDA UDI
Description: This equipment has been designed to be used to process signals from an endoscope and convert it to a signal that can be displayed on the monitor. FDA UDI

Identifiers

Primary DI / UDI-DI: 06971176280043 FDA UDI
510(k) Number: K190648 FDA UDI
FDA Product Code: FET FDA UDI
GMDN Term: Endoscopic video image processing unit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

MRI Safety

MR Unsafe FDA UDI

Category: Endoscopic video image processing unit

Eview by Zhuhai Pusen Medical Technology Co, Ltd — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Zhuhai Pusen Medical Technology Co, Ltd

Sources (1)

FDA UDI 6538898b-373d-448c-8335-dc6baf354d97 34 fields · synced Jun 1, 2026