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HWATO Vacuum Cupping Set

FDA UDI

Class I (US FDA UDI)

by Suzhou Medical Appliance Factory

Identity

Trade Name
HWATO Vacuum Cupping Set FDA UDI
Generic Name
Cupping therapy device FDA UDI
Device Name
Cupping therapy device: Vacuum Cupping Set, 18 PCS/Set FDA UDI
Model / Reference
18 PCS FDA UDI
Description
Cupping therapy device: Vacuum Cupping Set, 18 PCS/Set FDA UDI

Identifiers

Primary DI / UDI-DI
06901452150074 FDA UDI
FDA Product Code
KNM FDA UDI
GMDN Term
Cupping therapy device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5765 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cupping therapy device

HWATO Vacuum Cupping Set by Suzhou Medical Appliance Factory — 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 0cd68376-67c3-45cb-ad40-56513c7248a8 33 fields · synced May 30, 2026