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Persona

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Persona FDA UDI
Generic Name
Orthopaedic knee-balance analyser, non-electrical FDA UDI
Model / Reference
82-0153-183-00 FDA UDI

Identifiers

Catalog Number
82-0153-183-00 FDA UDI
Primary DI / UDI-DI
00889024492639 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Orthopaedic knee-balance analyser, non-electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic knee-balance analyser, non-electrical

Persona by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic knee-balance analyser, non-electrical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 8ff58ed7-833f-401c-8e31-f03bdc349aa9 34 fields · synced May 30, 2026