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BD MaxPlus

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
BD MaxPlus FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
Extension set, (minibore) with needleless connector 17.8 cm (7 in) FDA UDI
Model / Reference
MP2000 FDA UDI
Description
Extension set, (minibore) with needleless connector 17.8 cm (7 in) FDA UDI

Identifiers

Catalog Number
MP2000 FDA UDI
Primary DI / UDI-DI
10885403236532 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Intravenous administration tubing extension 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

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Intravenous administration tubing extension set

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

Similar devices

Also classified as Intravenous administration tubing extension 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 132503b5-a5a4-4924-a097-774ebf5a2631 37 fields · synced May 30, 2026