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Ascension®

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Ascension® FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Ascension® PIP Silicone MCP The Silicone MCP Lid is the top part of the case which locks onto the base and keeps content inside the base. FDA UDI
Model / Reference
CSA-500-01 FDA UDI
Description
Ascension® PIP Silicone MCP The Silicone MCP Lid is the top part of the case which locks onto the base and keeps content inside the base. FDA UDI

Identifiers

Catalog Number
CSA50001 FDA UDI
Primary DI / UDI-DI
10381780243793 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

Ascension® 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 fcc515ff-a6bd-447f-8f0c-ce4760b3aef5 36 fields · synced Jun 1, 2026