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Pen Needle

FDA UDI

Class II (US FDA UDI)

by Geri-Gentle Corporation

Identity

Trade Name
Pen Needle FDA UDI
Generic Name
Subcutaneous infusion/injection port needle FDA UDI
Device Name
Safety Pen Needle 30G FDA UDI
Model / Reference
11-305 FDA UDI
Description
Safety Pen Needle 30G FDA UDI

Identifiers

Primary DI / UDI-DI
00369771003390 FDA UDI
510(k) Number
K192677 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Subcutaneous infusion/injection port 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Subcutaneous infusion/injection port needle

Pen Needle by Geri-Gentle Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Subcutaneous infusion/injection port needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2867576c-1005-46ea-a9be-c68a923f40e9 34 fields · synced Jun 8, 2026