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Trinity Acetabular Hip System

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Trinity Acetabular Hip System FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
DRILL GUIDE FDA UDI
Model / Reference
921.108 FDA UDI
Description
DRILL GUIDE FDA UDI

Identifiers

Catalog Number
921.108 FDA UDI
Primary DI / UDI-DI
05055196970496 FDA UDI
510(k) Number
K093472 FDA UDI
FDA Product Code
MEH FDA UDI
LZO FDA UDI
LWJ FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3360 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: Surgical drill guide, reusable

Trinity Acetabular Hip System by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI e687eee9-4266-467f-a9a8-9eac833ec922 36 fields · synced May 30, 2026