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TM Ardis®

FDA UDI

Class II (US FDA UDI)

by Zimmer Trabecular Metal Technology, Inc.

Identity

Trade Name
TM Ardis® FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Model / Reference
96-701-31001 FDA UDI

Identifiers

Catalog Number
96-701-31001 FDA UDI
Primary DI / UDI-DI
00889024223813 FDA UDI
510(k) Number
K113561 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

TM Ardis® by Zimmer Trabecular Metal Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 091d6d43-3d74-4388-97cb-7434a856197c 35 fields · synced Jun 1, 2026