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Halyard

FDA UDI

Class II (US FDA UDI)

by Avid Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Orthopaedic surgical procedure kit, medicated FDA UDI
Model / Reference
JACK467-03_0003 FDA UDI

Identifiers

Catalog Number
JACK467-03 FDA UDI
Primary DI / UDI-DI
10809160468128 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic surgical procedure kit, medicated

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

Similar devices

Also classified as Orthopaedic surgical procedure kit, 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 b3323004-b85d-4fc2-8483-a446f4de0546 34 fields · synced Jun 8, 2026