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Yoke, Cga-960 X Cga-580 Female

FDA UDI

Class I (US FDA UDI)

by Bay Corporation

Identity

Trade Name
YOKE, CGA-960 X CGA-580 FEMALE FDA UDI
Generic Name
Pin-indexed adaptor, reusable FDA UDI
Device Name
YOKE, CGA-960 X CGA-580 FEMALE FDA UDI
Model / Reference
9601 FDA UDI
Description
YOKE, CGA-960 X CGA-580 FEMALE FDA UDI

Identifiers

Catalog Number
9601 FDA UDI
Primary DI / UDI-DI
B12896010 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

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: Pin-indexed adaptor, reusable

Yoke, Cga-960 X Cga-580 Female by Bay Corporation — 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

Manufacturer
Bay Corporation

Sources (1)

  • FDA UDI 8b457e3d-818b-4db9-a667-932a5d694153 35 fields · synced May 30, 2026