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Alaris

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
Alaris FDA UDI
Generic Name
Patient-controlled analgesia electric infusion pump administration set FDA UDI
Device Name
PCEA ASV YELLOW MICROBORE FDA UDI
Model / Reference
30893-07 FDA UDI
Description
PCEA ASV YELLOW MICROBORE FDA UDI

Identifiers

Catalog Number
30893-07 FDA UDI
Primary DI / UDI-DI
10885403460234 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Patient-controlled analgesia electric infusion pump administration set 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: Patient-controlled analgesia electric infusion pump administration set

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

Similar devices

Also classified as Patient-controlled analgesia electric infusion pump administration set.

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 bb3b28dd-3280-438e-81b3-38103ad44283 36 fields · synced May 30, 2026