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Halyard

FDA UDI

Class II (US FDA UDI)

by Avid Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Peripheral anaesthesia single-administration set, non-medicated FDA UDI
Model / Reference
CNPD034_0012 FDA UDI

Identifiers

Catalog Number
CNPD034 FDA UDI
Primary DI / UDI-DI
10809160357613 FDA UDI
FDA Product Code
OGD FDA UDI
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral anaesthesia single-administration set, non-medicated

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

Similar devices

Also classified as Peripheral anaesthesia single-administration set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avid Medical, Inc.

Sources (1)

  • FDA UDI 82289c56-c3d6-4bb8-ac15-501e0130acae 34 fields · synced Jun 8, 2026