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Tuohy

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
TUOHY FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
Tuohy-Kanüle FDA UDI
Model / Reference
1150-4M090 FDA UDI
Description
Tuohy-Kanüle FDA UDI

Identifiers

Catalog Number
1150-4M090 FDA UDI
Primary DI / UDI-DI
04048223115688 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Epidural needle, non-threaded 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 90.0 Millimeter FDA UDI
Outer Diameter — 1.4 Millimeter FDA UDI

Category: Epidural needle, non-threaded

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

Similar devices

Also classified as Epidural needle, non-threaded.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76398bd1-e07c-4df9-b0c7-2e3d36d12e92 37 fields · synced May 30, 2026