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Nutriline Twinflo

FDA UDI

Class II (US FDA UDI)

by Vygon Corp.

Identity

Trade Name
Nutriline Twinflo FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
NUTRLINE TWINFLOW 24 G (2FR) 30 CM DUAL LUMEN CATHETER FDA UDI
Model / Reference
1252.232G FDA UDI
Description
NUTRLINE TWINFLOW 24 G (2FR) 30 CM DUAL LUMEN CATHETER FDA UDI

Identifiers

Catalog Number
1252.232G FDA UDI
Primary DI / UDI-DI
08498840009451 FDA UDI
510(k) Number
K052475 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Peripherally-inserted central venous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 24 Millimeter FDA UDI

Category: Peripherally-inserted central venous catheter

Nutriline Twinflo by Vygon Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Cleared under the same submission

K052475 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vygon Corp.

Sources (1)

  • FDA UDI 3127f3cc-2c00-4d31-882e-16e2064a5b27 37 fields · synced Jun 1, 2026