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Good Sense Pen Needles

FDA UDI

Class II (US FDA UDI)

by L Perrigo Company

Identity

Trade Name
Good Sense Pen Needles FDA UDI
Generic Name
Autoinjector needle FDA UDI
Device Name
Sterile, single-use, 6-bevel pen needles, 31 Gauge, 8mm (5/16") Length, extra-thin wall FDA UDI
Model / Reference
700014726 FDA UDI
Description
Sterile, single-use, 6-bevel pen needles, 31 Gauge, 8mm (5/16") Length, extra-thin wall FDA UDI

Identifiers

Primary DI / UDI-DI
00370030125357 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Autoinjector needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Yes

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
Needle Gauge — 31 Gauge FDA UDI
Length — 8 Millimeter FDA UDI

Category: Autoinjector needle

Good Sense Pen Needles by L Perrigo Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autoinjector needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
L Perrigo Company

Sources (1)

  • FDA UDI 3b6a2a76-9469-43f8-badf-aa53dbd4ef48 34 fields · synced May 29, 2026