Creliver

FDA UDI

Class II (US FDA UDI)

by Shenzhen Osto Technology Co., Ltd.

Identity

Trade Name: Creliver FDA UDI
Generic Name: Acupuncture electrical stimulation system FDA UDI
Model / Reference: AST-623B FDA UDI

Identifiers

Primary DI / UDI-DI: 06950940802049 FDA UDI
510(k) Number: K211942 FDA UDI
FDA Product Code: IRT FDA UDI
NGX FDA UDI
NUH FDA UDI
GMDN Term: Acupuncture electrical stimulation system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5740 FDA UDI
890.5850 FDA UDI
882.5890 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Acupuncture electrical stimulation system

Creliver by Shenzhen Osto 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: Shenzhen Osto Technology Co., Ltd.

Sources (1)

FDA UDI dcc1a7b3-bb9f-425f-8f42-f55bec49e833 33 fields · synced Jun 8, 2026