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Glass Cup Flat Top No.2

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DY2040

by Tens Plus Industrial Company

Identity

Trade Name
GLASS CUP FLAT TOP NO.2 FDA UDI
Generic Name
Cupping therapy device FDA UDI
Device Name
Vacuum cupping and Tools EUDAMED
Model / Reference
DY2040 EUDAMED
FireCup.2M FDA UDI

Identifiers

Primary DI / UDI-DI
14897076721310 EUDAMEDFDA UDI
Basic UDI-DI
489707672DAZTX EUDAMED
FDA Product Code
KNM FDA UDI
EMDN Code
Z120611 VACUUM THERAPY EQUIPMENT EUDAMED
GMDN Term
Cupping therapy device FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.5765 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Category: Cupping therapy device

Glass Cup Flat Top No.2 by Tens Plus Industrial Company — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cupping therapy device.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI fb8e5cdf-5a4a-48d1-b417-42c64d7a5660 32 fields · synced Jun 19, 2026
  • EUDAMED 600f1154-430a-41fd-b56b-92524f089134 61 fields · synced Jun 19, 2026