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Devon

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Devon FDA UDI
Generic Name
Birthing/delivery kit FDA UDI
Device Name
7329-HRZ Delivery Kit FDA UDI
Model / Reference
56472 FDA UDI
Description
7329-HRZ Delivery Kit FDA UDI

Identifiers

Catalog Number
56472 FDA UDI
Primary DI / UDI-DI
20884527007704 FDA UDI
FDA Product Code
MLS FDA UDI
GMDN Term
Birthing/delivery kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Birthing/delivery kit

Devon by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Birthing/delivery kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI b463f700-fcf1-4915-8e58-6d80f2375c1f 36 fields · synced May 31, 2026