Adapter

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name: Adapter FDA UDI
Generic Name: Closed-wound drain connection tubing set FDA UDI
Device Name: Small Blue Adapter, for use with ReliaVac 400 and ReliaVac 100 Closed Wound Suction Systems and 1/8" Round Silicone Drains FDA UDI
Model / Reference: 9019500 FDA UDI
Description: Small Blue Adapter, for use with ReliaVac 400 and ReliaVac 100 Closed Wound Suction Systems and 1/8" Round Silicone Drains FDA UDI

Identifiers

Catalog Number: 9019500 FDA UDI
Primary DI / UDI-DI: 10801741051385 FDA UDI
FDA Product Code: GCY FDA UDI
GMDN Term: Closed-wound drain connection tubing set FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4680 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Closed-wound drain connection tubing set

Adapter by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: C. R. Bard, Inc.

Sources (1)

FDA UDI cd138b1c-9b21-403d-a940-706fc4fca89e 35 fields · synced May 31, 2026