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Baxject Ii

FDA UDIEUDAMED

Class II (US FDA UDI)

by Takeda Pharmaceuticals U.S.A., Inc.

Identity

Trade Name
BAXJECT II FDA UDI
Generic Name
Medication transfer set FDA UDI
Device Name
Needleless Transfer Device FDA UDI
Model / Reference
6507816 FDA UDI
Description
Needleless Transfer Device FDA UDI

Identifiers

Catalog Number
6507816 FDA UDI
Primary DI / UDI-DI
00850025688864 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Medication transfer 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: Medication transfer set

Baxject Ii by Takeda Pharmaceuticals U.S.A., Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer set.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI b4884321-981d-4df1-b39d-69be9a2ffe7f 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026