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Power-Flo®

FDA UDI

Class I (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
Power-Flo® FDA UDI
Generic Name
Manual orthopaedic cement mixer, single-use FDA UDI
Model / Reference
00-5049-045-01 FDA UDI

Identifiers

Catalog Number
00-5049-045-01 FDA UDI
Primary DI / UDI-DI
00889024374850 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

Power-Flo® by Zimmer Orthopaedic Surgical Products — 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 7664373b-3272-4466-89d3-4407880821bd 34 fields · synced Jun 8, 2026