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Aiv

FDA UDI

Class II (US FDA UDI)

by American I.v. Products, Inc.

Identity

Trade Name
AIV FDA UDI
Generic Name
Bedside syringe pump FDA UDI
Device Name
L02 Smart Label Propofol FDA UDI
Model / Reference
BX12812 FDA UDI
Description
L02 Smart Label Propofol FDA UDI

Identifiers

Catalog Number
BX12812 FDA UDI
Primary DI / UDI-DI
M745BX12812 FDA UDI
510(k) Number
K142333 FDA UDI
FDA Product Code
MRZ FDA UDI
GMDN Term
Bedside syringe pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 2.315 Inch FDA UDI
Length — 5.95 Inch FDA UDI

Category: Bedside syringe pump

Aiv by American I.v. Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside syringe pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
American I.v. Products, Inc.

Sources (1)

  • FDA UDI b4d37e20-377c-4912-a2fc-ca50acbc636e 36 fields · synced Jun 8, 2026