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Gel warmer

FDA UDI

Class II (US FDA UDI)

by Shenzhen Wisonic Medical Technology Co., Ltd.

Identity

Trade Name
Gel warmer FDA UDI
Generic Name
Gel warmer FDA UDI
Model / Reference
UGW-01 FDA UDI

Identifiers

Primary DI / UDI-DI
06971355420796 FDA UDI
510(k) Number
K210154 FDA UDI
FDA Product Code
IYN FDA UDI
GMDN Term
Gel warmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Gel warmer

Gel warmer by Shenzhen Wisonic Medical Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gel warmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8da312ba-a96c-462b-960d-552b0dc593f4 33 fields · synced May 30, 2026