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Cleanest

FDA UDI

Class I (US FDA UDI)

by Guangzhou Clean Medical Products Manufacturing Corp.

Identity

Trade Name
CLEANEST FDA UDI
Generic Name
Manual orthopaedic cement mixer, single-use FDA UDI
Device Name
Large Nozzle [Accessory for Bone Cement Mixing System] FDA UDI
Model / Reference
CL006-06-17E FDA UDI
Description
Large Nozzle [Accessory for Bone Cement Mixing System] FDA UDI

Identifiers

Primary DI / UDI-DI
06951233721788 FDA UDI
FDA Product Code
JDZ FDA UDI
GMDN Term
Manual orthopaedic cement mixer, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual orthopaedic cement mixer, single-use

Cleanest by Guangzhou Clean Medical Products Manufacturing Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual orthopaedic cement mixer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d7183be-b467-4a8a-89a2-9a98dc1b763b 33 fields · synced May 30, 2026