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WiScope

FDA UDI

Class II (US FDA UDI)

by Jiangsu Jiyuan Medical Technology Co., Ltd

Identity

Trade Name
WiScope FDA UDI
Generic Name
Rigid video hysteroscope FDA UDI
Device Name
Single-Use Digital Hysteroscope FDA UDI
Model / Reference
OTU-HJ01 FDA UDI
Description
Single-Use Digital Hysteroscope FDA UDI

Identifiers

Primary DI / UDI-DI
06973672290410 FDA UDI
FDA Product Code
HIH FDA UDI
GMDN Term
Rigid video hysteroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid video hysteroscope

WiScope by Jiangsu Jiyuan Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid video hysteroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06d2bb6b-3049-4715-8007-c3753c7c00d2 34 fields · synced Jun 8, 2026