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Pro Nozzle short with knee pressurizer

FDA UDI

Class I (US FDA UDI)

by Heraeus Medical LLC

Identity

Trade Name
Pro Nozzle short with knee pressurizer FDA UDI
Generic Name
Manual orthopaedic cement mixer, reusable FDA UDI
Device Name
The Pro Nozzle short with knee pressurizer is used in combination with the Pro bone cement system FDA UDI
Model / Reference
66057202 FDA UDI
Description
The Pro Nozzle short with knee pressurizer is used in combination with the Pro bone cement system FDA UDI

Identifiers

Primary DI / UDI-DI
04260102133099 FDA UDI
FDA Product Code
KIH FDA UDI
GMDN Term
Manual orthopaedic cement mixer, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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, reusable

Pro Nozzle short with knee pressurizer by Heraeus Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual orthopaedic cement mixer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Heraeus Medical LLC

Sources (1)

  • FDA UDI 8731e42b-c38e-43a5-acc4-2d1e976a99ed 33 fields · synced May 30, 2026