← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Negative-pressure intravenous line needleless valve-connector FDA UDI
Device Name
SMARTSITE, NEGATIVE DISPLACEMENT VALVE FDA UDI
Model / Reference
DYNDTC2000A FDA UDI
Description
SMARTSITE, NEGATIVE DISPLACEMENT VALVE FDA UDI

Identifiers

Catalog Number
DYNDTC2000A FDA UDI
Primary DI / UDI-DI
10884389719732 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

Medline by Medline Industries, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 11a10821-a491-4147-8456-afbbf48355c4 35 fields · synced Jun 6, 2026