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Cordera Hip System Acetabular Reusable Instrument Tray, insert and base

FDA UDI

Class I (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
Cordera Hip System Acetabular Reusable Instrument Tray, insert and base FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Acetabular Reusable Instrument Tray, insert and base FDA UDI
Model / Reference
1080-121 FDA UDI
Description
Acetabular Reusable Instrument Tray, insert and base FDA UDI

Identifiers

Catalog Number
1080-121 FDA UDI
Primary DI / UDI-DI
00810933031251 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Instrument tray, reusable

Cordera Hip System Acetabular Reusable Instrument Tray, insert and base by Conformis, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI f22f3b15-7d7c-4b93-b32d-585e970f1c6d 35 fields · synced May 30, 2026