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Cordera Hip System

FDA UDI

Class I (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
Cordera Hip System FDA UDI
Generic Name
Orthopaedic x-ray reference grid FDA UDI
Device Name
Cordera Cup Acetate - 110% Magnification Template FDA UDI
Model / Reference
1080-665 FDA UDI
Description
Cordera Cup Acetate - 110% Magnification Template FDA UDI

Identifiers

Catalog Number
1080-665 FDA UDI
Primary DI / UDI-DI
00810933031343 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Orthopaedic x-ray reference grid FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Orthopaedic x-ray reference grid

Cordera Hip System by Conformis, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic x-ray reference grid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI b15d4c09-b708-4896-b55e-15fb303f6b57 35 fields · synced May 30, 2026