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SPROTTE® NRFit

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
SPROTTE® NRFit FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
SPROTTE® NRFit 24G x 31/2" (90mm) with magnification sterile FDA UDI
Model / Reference
001163-30A FDA UDI
Description
SPROTTE® NRFit 24G x 31/2" (90mm) with magnification sterile FDA UDI

Identifiers

Catalog Number
001163-30A FDA UDI
Primary DI / UDI-DI
04048223130766 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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

Dimensions & Sizes

Size
Outer Diameter — 0.55 Millimeter FDA UDI
Length — 90.0 Millimeter FDA UDI

Category: Spinal needle, single-use

SPROTTE® NRFit by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal needle, single-use.

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 43f4896b-3c27-4ced-bdac-b768ebdf1bf1 37 fields · synced Jun 1, 2026