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PlexoLong NanoLine® acc. Meier

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
PlexoLong NanoLine® acc. Meier FDA UDI
Generic Name
Peripheral anaesthesia catheter set, non-medicated FDA UDI
Device Name
PlexoLong NanoLine® acc. Meier PlexoLong NanoLine® cannula 18G x 50mm with Tuohy tip, Luer Lock FDA UDI
Model / Reference
531156-31C FDA UDI
Description
PlexoLong NanoLine® acc. Meier PlexoLong NanoLine® cannula 18G x 50mm with Tuohy tip, Luer Lock FDA UDI

Identifiers

Catalog Number
531156-31C FDA UDI
Primary DI / UDI-DI
04048223126455 FDA UDI
510(k) Number
K053283 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Peripheral anaesthesia catheter set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peripheral anaesthesia catheter set, non-medicated

PlexoLong NanoLine® acc. Meier by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral anaesthesia catheter set, non-medicated.

Cleared under the same submission

K053283 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pajunk GmbH Medizintechnologie

Sources (1)

  • FDA UDI d70e9680-d9a2-4708-9001-08fa54cf3c0a 37 fields · synced May 30, 2026