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AccuTip

FDA UDI

Class II (US FDA UDI)

by Clint Pharmaceuticals, Inc.

Identity

Trade Name
AccuTip FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
Detachable Wing Epidural Needle FDA UDI
Model / Reference
AT18G60T FDA UDI
Description
Detachable Wing Epidural Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00817781020222 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 — 6 Inch FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: Epidural needle, non-threaded

AccuTip by Clint Pharmaceuticals, 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 e4fab6f9-08d3-4999-b561-3cdd36c0cf0d 34 fields · synced May 30, 2026