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Integra®

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Integra® FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Integra® Total Foot System The Tarsalis Plate Caddy Inset is a separate container that rests within the base of the caddy. It is used to contain items. FDA UDI
Model / Reference
CSA-805-03 FDA UDI
Description
Integra® Total Foot System The Tarsalis Plate Caddy Inset is a separate container that rests within the base of the caddy. It is used to contain items. FDA UDI

Identifiers

Catalog Number
CSA80503 FDA UDI
Primary DI / UDI-DI
10381780244134 FDA UDI
FDA Product Code
OJH FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Integra® by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b9157ba4-0657-4362-95bf-d4e51ae95563 36 fields · synced May 31, 2026