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Tiger Warmer Large

FDA UDI

Class I (US FDA UDI)

by Dong Bang Medical co., Ltd.

Identity

Trade Name
Tiger Warmer Large FDA UDI
Generic Name
Cupping therapy device FDA UDI
Model / Reference
DB 215C FDA UDI

Identifiers

Primary DI / UDI-DI
18800018916428 FDA UDI
FDA Product Code
IMA FDA UDI
GMDN Term
Cupping therapy device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5730 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cupping therapy device

Tiger Warmer Large by Dong Bang Medical co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cupping therapy device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 26be2d29-e80f-4316-bb07-403285b4c57e 32 fields · synced May 30, 2026