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Mezut

FDA UDI

Class I (US FDA UDI)

by Shanghai Jianying Medical Technology Co., Ltd.

Identity

Trade Name
MEZUT FDA UDI
Generic Name
Headband, reusable FDA UDI
Model / Reference
W003 FDA UDI

Identifiers

Primary DI / UDI-DI
06972176090052 FDA UDI
FDA Product Code
BTK FDA UDI
GMDN Term
Headband, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5560 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Headband, reusable

Mezut by Shanghai Jianying Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Headband, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a864fb2d-ada9-4427-a806-ade311e4fba8 32 fields · synced Jun 1, 2026