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Interlink

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
INTERLINK FDA UDI
Generic Name
Vial/bottle adaptor, hermetic FDA UDI
Device Name
Universal Vial Adapter FDA UDI
Model / Reference
2N3395 FDA UDI
Description
Universal Vial Adapter FDA UDI

Identifiers

Catalog Number
2N3395 FDA UDI
Primary DI / UDI-DI
00085412004976 FDA UDI
510(k) Number
K924064 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Vial/bottle adaptor, hermetic 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: Vial/bottle adaptor, hermetic

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

Similar devices

Also classified as Vial/bottle adaptor, hermetic.

Cleared under the same submission

K924064 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0b1e60c-e55f-4a84-82a7-90e4fc79fd79 36 fields · synced May 31, 2026