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Omnia Medical Coupler-C

FDA UDI

Class II (US FDA UDI)

by Omnia Medical

Identity

Trade Name
Omnia Medical Coupler-C FDA UDI
Generic Name
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
PLATE HOLDER FDA UDI
Model / Reference
15-5C-PHR1 FDA UDI
Description
PLATE HOLDER FDA UDI

Identifiers

Catalog Number
15-5C-PHR1 FDA UDI
Primary DI / UDI-DI
00843511113582 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Surgical implant/trial-implant/sizer holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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 implant/trial-implant/sizer holder, reusable

Omnia Medical Coupler-C by Omnia Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant/trial-implant/sizer holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Omnia Medical

Sources (1)

  • FDA UDI 1bbcf094-ab9b-476e-aaf4-1d2cb5a65e88 35 fields · synced May 30, 2026