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Vial-Mate

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
VIAL-MATE FDA UDI
Generic Name
Medication transfer set FDA UDI
Device Name
VIAL-MATE Adaptor FDA UDI
Model / Reference
2B8071 FDA UDI
Description
VIAL-MATE Adaptor FDA UDI

Identifiers

Catalog Number
2B8071 FDA UDI
Primary DI / UDI-DI
00085412027388 FDA UDI
510(k) Number
K142600 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medication transfer set

Vial-Mate by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b95dafa-5ca6-43a5-93f2-4aafbed94890 36 fields · synced Jun 8, 2026