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Alaris, SmartSite

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
Alaris, SmartSite FDA UDI
Generic Name
Intra-abdominal pressure measurement set, electronic FDA UDI
Device Name
20mm Vial Access Device, Needle-free Valve, 3.5 cm (1.5 in) FDA UDI
Model / Reference
2205E FDA UDI
Description
20mm Vial Access Device, Needle-free Valve, 3.5 cm (1.5 in) FDA UDI

Identifiers

Catalog Number
2205E FDA UDI
Primary DI / UDI-DI
07613203011778 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Intra-abdominal pressure measurement set, electronic 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 — 1.5 Inch FDA UDI

Category: Electric infusion pump administration set, single-useIntra-abdominal pressure measurement set, electronic

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

Similar devices

Also classified as Intra-abdominal pressure measurement set, electronic.

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 4c44f4ab-d581-4655-88eb-39feae013dcd 37 fields · synced May 30, 2026