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Truwave

FDA UDI

Class II (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
TRUWAVE FDA UDI
Generic Name
Luer/Luer linear connector, single-use FDA UDI
Device Name
4 PORT CONNECTOR STERILE FDA UDI
Model / Reference
MK2458 FDA UDI
Description
4 PORT CONNECTOR STERILE FDA UDI

Identifiers

Catalog Number
MK2458 FDA UDI
Primary DI / UDI-DI
07460691957640 FDA UDI
510(k) Number
K142749 FDA UDI
FDA Product Code
DXO FDA UDI
GMDN Term
Luer/Luer linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2870 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

Yes

FDA UDI

Category: Luer/Luer linear connector, single-use

Truwave by Edwards Lifesciences LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/Luer linear connector, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 311998ff-2600-493d-9abf-e6170843a28a 37 fields · synced Jun 8, 2026