← Back to catalogue

Alaris, VersaSafe

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
Alaris, VersaSafe FDA UDI
Generic Name
Neutral-pressure intravenous line needleless valve-connector FDA UDI
Device Name
Split Septum Connector FDA UDI
Model / Reference
1000M FDA UDI
Description
Split Septum Connector FDA UDI

Identifiers

Catalog Number
1000M FDA UDI
Primary DI / UDI-DI
10885403226076 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Neutral-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

Dimensions & Sizes

Size
Length — 0.75 Inch FDA UDI

Category: Neutral-pressure intravenous line needleless valve-connector

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
BD Switzerland Sàrl

Sources (1)

  • FDA UDI 8c2f72cf-481c-4e90-9447-3057b0291da2 37 fields · synced May 30, 2026