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Moxa.Bx.BamS

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref GY5337

by Tens Plus Industrial Company

Identity

Trade Name
Moxa.Bx.BamS FDA UDI
Generic Name
Moxibustion container FDA UDI
Device Name
Moxa Tools EUDAMED
Model / Reference
GY5337 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
14897076721815 EUDAMEDFDA UDI
Basic UDI-DI
489707672GACSY EUDAMED
FDA Product Code
KNM FDA UDI
EMDN Code
Z12069099 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER EUDAMED
GMDN Term
Moxibustion container 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: Moxibustion container

Moxa.Bx.BamS by Tens Plus Industrial Company — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Moxibustion container.

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 bc987c2b-0621-449b-ac1b-8724ce20e4b7 32 fields · synced Jun 18, 2026
  • EUDAMED d875a0d2-859d-4136-96b6-1822b2c0d1b9 61 fields · synced Jun 18, 2026