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Tuohy Epidural Needle

FDA UDI

Class II (US FDA UDI)

by Remington Medical, Inc.

Identity

Trade Name
Tuohy Epidural Needle FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
17 ga (1.4mm) x 13 cm FDA UDI
Model / Reference
TNMF-1705 FDA UDI
Description
17 ga (1.4mm) x 13 cm FDA UDI

Identifiers

Catalog Number
TNMF-1705 FDA UDI
Primary DI / UDI-DI
00813079021001 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

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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 17 Gauge FDA UDI

Category: Epidural needle, non-threaded

Tuohy Epidural Needle by Remington Medical, Inc. — 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

Manufacturer
Remington Medical, Inc.

Sources (1)

  • FDA UDI 7c5d0acb-06d7-4041-850b-209a9fe02079 36 fields · synced Jun 8, 2026