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Future Generation Medical

FDA UDI

Class II (US FDA UDI)

by Global International L. L. C.

Identity

Trade Name
Future Generation Medical FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
Safety Syringes 1ml with 25G x 1in FDA UDI
Model / Reference
F12510GM FDA UDI
Description
Safety Syringes 1ml with 25G x 1in FDA UDI

Identifiers

Primary DI / UDI-DI
10850046230087 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: General-purpose syringe/needle

Future Generation Medical by Global International L. L. C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11a47939-2920-4667-9a8d-6136448cce44 34 fields · synced Jun 6, 2026