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MaxGuard

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
MaxGuard FDA UDI
Generic Name
Negative-pressure intravenous line needleless valve-connector FDA UDI
Device Name
TRU-SWAB MAX CONNECTOR OPAQ FDA UDI
Model / Reference
MX1002 FDA UDI
Description
TRU-SWAB MAX CONNECTOR OPAQ FDA UDI

Identifiers

Catalog Number
MX1002 FDA UDI
Primary DI / UDI-DI
10885403237447 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Negative-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

Category: Negative-pressure intravenous line needleless valve-connector

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

Similar devices

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

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 796e1e5b-4377-4ab5-a1a9-a6f52dd61386 36 fields · synced May 31, 2026