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iCare Vacuum Cupping Set

FDA UDI

Class I (US FDA UDI)

by Prime Holly Corporation

Identity

Trade Name
iCare Vacuum Cupping Set FDA UDI
Generic Name
Cupping therapy device FDA UDI
Device Name
iCare Vacuum Cupping Set FDA UDI
Model / Reference
CC200 FDA UDI
Description
iCare Vacuum Cupping Set FDA UDI

Identifiers

Catalog Number
CC200 FDA UDI
Primary DI / UDI-DI
00818318025352 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cupping therapy device

iCare Vacuum Cupping Set by Prime Holly Corporation — 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 109f3917-a094-4816-a0f5-f41c782833f1 35 fields · synced May 30, 2026