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Pain Relief Patch

FDA UDI

Class I (US FDA UDI)

by Hunan Jianyuan Medical Science And Technology Co., Ltd.

Identity

Trade Name
Pain Relief Patch FDA UDI
Generic Name
Transdermal medication patch FDA UDI
Model / Reference
JYT-A FDA UDI

Identifiers

Primary DI / UDI-DI
06959962439011 FDA UDI
FDA Product Code
OMW FDA UDI
GMDN Term
Transdermal medication patch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Transdermal medication patch

Pain Relief Patch by Hunan Jianyuan Medical Science And Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transdermal medication patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hunan Jianyuan Medical Science And Technology Co., Ltd.

Sources (1)

  • FDA UDI d8cac61b-dac8-4864-87ee-19d620744381 32 fields · synced May 30, 2026