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Doctors Choice

FDA UDI

Class II (US FDA UDI)

by Supply Line International Medical, LLC

Identity

Trade Name
Doctors Choice FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Safety Needle, 25G x 1" FDA UDI
Model / Reference
SND25G0102 FDA UDI
Description
Safety Needle, 25G x 1" FDA UDI

Identifiers

Primary DI / UDI-DI
G018SND25G01020 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use 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

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

Yes

FDA UDI

Category: Hypodermic needle, single-use

Doctors Choice by Supply Line International Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e5e392d-5fbf-4d50-88f8-f3500677ed9a 33 fields · synced May 29, 2026