← Back to catalogue

New Moxa Stick

FDA UDI

Class I (US FDA UDI)

by Yamasho Co., Ltd.

Identity

Trade Name
NEW MOXA STICK FDA UDI
Generic Name
Moxa FDA UDI
Model / Reference
10pcs FDA UDI

Identifiers

Primary DI / UDI-DI
04979844700116 FDA UDI
FDA Product Code
IMA FDA UDI
GMDN Term
Moxa 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Moxa

New Moxa Stick by Yamasho Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Moxa.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Yamasho Co., Ltd.

Sources (1)

  • FDA UDI 4c77cd69-ff18-4a59-8fa5-ff11ed79cf75 32 fields · synced May 30, 2026