← Back to catalogue

Halyard

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Peripheral anaesthesia catheter set, non-medicated FDA UDI
Device Name
HYH,UBLOCK,UBT,-,-,10 FDA UDI
Model / Reference
92960 FDA UDI
Description
HYH,UBLOCK,UBT,-,-,10 FDA UDI

Identifiers

Catalog Number
181126 FDA UDI
Primary DI / UDI-DI
10680651929607 FDA UDI
510(k) Number
K941153 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Peripheral anaesthesia catheter set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral anaesthesia catheter set, non-medicated

Halyard by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral anaesthesia catheter set, non-medicated.

Cleared under the same submission

K941153 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI c4d757a3-93cb-4ab3-b981-3f25b379ab81 36 fields · synced Jun 9, 2026