Shinva

FDA UDI

Class I (US FDA UDI)

by Xinhua Surgical Instrument Co., Ltd.

Identity

Trade Name: Shinva FDA UDI
Generic Name: General-purpose surgical scissors, reusable FDA UDI
Device Name: MIS root elevator 3#, 3mm, straight blade FDA UDI
Model / Reference: ZR1363RB FDA UDI
Description: MIS root elevator 3#, 3mm, straight blade FDA UDI

Identifiers

Primary DI / UDI-DI: 06936894733837 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: General-purpose surgical scissors, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: General-purpose surgical scissors, reusable

Shinva by Xinhua Surgical Instrument Co., Ltd. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Xinhua Surgical Instrument Co., Ltd.

Sources (1)

FDA UDI d9fe6fad-983f-4919-82c4-3aa43928032f 33 fields · synced May 29, 2026