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Halyard

FDA UDI

Class II (US FDA UDI)

by Avid Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Vascular catheterization support/maintenance kit, non-medicated FDA UDI
Model / Reference
WRNM025-06_0005 FDA UDI

Identifiers

Catalog Number
WRNM025-06 FDA UDI
Primary DI / UDI-DI
10809160338124 FDA UDI
FDA Product Code
OEZ FDA UDI
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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: Vascular catheterization support/maintenance kit, non-medicated

A comprehensive medical device directory listing for the Halyard vascular catheterization support/maintenance kit, a non-medicated device designed to assist with patient care and maintenance.

Similar devices

Also classified as Vascular catheterization support/maintenance kit, 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 8d427a49-a4c9-44b6-9a52-071abcb98aab 34 fields · synced Jul 16, 2026