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Mixer

FDA UDIEUDAMED

Class I (US FDA UDI)

by Joline GmbH & Co. KG

Identity

Trade Name
Mixer FDA UDI
Generic Name
Manual orthopaedic cement mixer, single-use FDA UDI
Model / Reference
US9610 FDA UDI

Identifiers

Primary DI / UDI-DI
04250203940917 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

Yes

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

Mixer by Joline GmbH & Co. KG — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

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 919df560-6eaf-40aa-bf43-697a8e58b191 32 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026