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Dover

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Dover FDA UDI
Generic Name
Non-ISO80369-standardized small-bore linear connector, reusable FDA UDI
Device Name
VINYL URETHRAL CATHETER, FEMALE, SMOOTH ROUNDED TIP, 14 FR (4.7 MM) X 6.5" (16 CM) LENGTH FDA UDI
Model / Reference
8887660903 FDA UDI
Description
VINYL URETHRAL CATHETER, FEMALE, SMOOTH ROUNDED TIP, 14 FR (4.7 MM) X 6.5" (16 CM) LENGTH FDA UDI

Identifiers

Catalog Number
8887660903 FDA UDI
Primary DI / UDI-DI
10192253030303 FDA UDI
FDA Product Code
KOD FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore linear connector, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6.5 Inch FDA UDI
Catheter Gauge — 14 French FDA UDI

Category: Non-ISO80369-standardized small-bore linear connector, reusable

Dover by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-ISO80369-standardized small-bore linear connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 97f05d11-e54b-4821-b9aa-f012bd4886c4 35 fields · synced Jun 8, 2026