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Mediwish

FDA UDI

Class I (US FDA UDI)

by Mediwish Co., Ltd

Identity

Trade Name
Mediwish FDA UDI
Generic Name
Dental-professional prophylaxis brush, single-use FDA UDI
Model / Reference
2.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
06974409699681 FDA UDI
FDA Product Code
KXF FDA UDI
GMDN Term
Dental-professional prophylaxis brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental-professional prophylaxis brush, single-use

Mediwish by Mediwish Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental-professional prophylaxis brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mediwish Co., Ltd

Sources (1)

  • FDA UDI a037877f-acad-4738-b814-903180c6a6bc 32 fields · synced May 30, 2026