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Superior Products Inc

FDA UDI

Class I (US FDA UDI)

by Superior Products, LLC

Identity

Trade Name
Superior Products Inc FDA UDI
Generic Name
Pin-indexed adaptor, reusable FDA UDI
Device Name
CGA-950 YOKE W/ VITON WASHER FDA UDI
Model / Reference
Medical Yokes FDA UDI
Description
CGA-950 YOKE W/ VITON WASHER FDA UDI

Identifiers

Catalog Number
0987-0179 FDA UDI
Primary DI / UDI-DI
00747252002535 FDA UDI
FDA Product Code
CAM FDA UDI
GMDN Term
Pin-indexed adaptor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6885 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

No

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: Pin-indexed adaptor, reusable

Superior Products Inc by Superior Products, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin-indexed adaptor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 83d51cc6-c5ae-42c6-929e-d9c3bff97676 34 fields · synced May 30, 2026