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Biotronix Healthcare Syringes

FDA UDI

Class II (US FDA UDI)

by Biotronix Healthcare Industries Inc.

Identity

Trade Name
Biotronix Healthcare Syringes FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
Disposable 1CC Insulin Unibody Syringe, U-100, Needle 31G x 5/16" FDA UDI
Model / Reference
GE12004-R FDA UDI
Description
Disposable 1CC Insulin Unibody Syringe, U-100, Needle 31G x 5/16" FDA UDI

Identifiers

Primary DI / UDI-DI
00858835007400 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Insulin syringe/needle, basic 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

Yes

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

Category: Insulin syringe/needle, basic

Biotronix Healthcare Syringes by Biotronix Healthcare Industries Inc. — 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

Sources (1)

  • FDA UDI 0a9a2c53-e8ab-4d25-b4ae-900ba0472e0d 36 fields · synced May 30, 2026