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DropSafe Safety Needle

FDA UDI

Class II (US FDA UDI)

by Htl Strefa S A

Identity

Trade Name
DropSafe Safety Needle FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
The sterile Safety Needle is intended for use in the aspiration and injection of fluids for medical purpose. FDA UDI
Model / Reference
23G FDA UDI
Description
The sterile Safety Needle is intended for use in the aspiration and injection of fluids for medical purpose. FDA UDI

Identifiers

Catalog Number
6060 FDA UDI
Primary DI / UDI-DI
85907996099326 FDA UDI
FDA Product Code
MEG FDA UDI
FMF FDA UDI
FMI FDA UDI
GMDN Term
Insulin syringe/needle, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
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

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

Category: Insulin syringe/needle, basic

DropSafe Safety Needle by Htl Strefa S A — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin syringe/needle, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Htl Strefa S A

Sources (1)

  • FDA UDI f4a18d79-2508-4ddb-9679-a57326f1997b 34 fields · synced May 30, 2026