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VersaSafe

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
VersaSafe FDA UDI
Generic Name
Positive-pressure intravenous line needleless valve-connector FDA UDI
Device Name
VersaSafe Plastic Cannula FDA UDI
Model / Reference
9391-0200 FDA UDI
Description
VersaSafe Plastic Cannula FDA UDI

Identifiers

Catalog Number
9391-0200 FDA UDI
Primary DI / UDI-DI
07613203009515 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Positive-pressure intravenous line needleless valve-connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Positive-pressure intravenous line needleless valve-connector

VersaSafe by BD Switzerland Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Positive-pressure intravenous line needleless valve-connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BD Switzerland Sàrl

Sources (1)

  • FDA UDI 0d1cfa2d-f53d-44a9-8f85-f58daea3cc5c 36 fields · synced Jun 1, 2026