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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
NDL,TUOHY EPID,17GX3.5",PLASTIC STYLET FDA UDI
Model / Reference
PAIN8001 FDA UDI
Description
NDL,TUOHY EPID,17GX3.5",PLASTIC STYLET FDA UDI

Identifiers

Catalog Number
PAIN8001 FDA UDI
Primary DI / UDI-DI
10884389619971 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

Dimensions & Sizes

Size
Length — 3.5 Inch FDA UDI

Category: Epidural needle, non-threaded

Medline by Medline Industries, 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

Sources (1)

  • FDA UDI 7d742aa3-d118-4be8-891c-a66287f34d2d 37 fields · synced May 30, 2026