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Syringe LL, W/BioCare Safety Needle

FDA UDI

Class II (US FDA UDI)

by Biotronix Healthcare Industries Inc.

Identity

Trade Name
Syringe LL, W/BioCare Safety Needle FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Disposable 3cc Syringe LL, W/BioGuard Safety Needle 21G x 1" FDA UDI
Model / Reference
BIO-1051S FDA UDI
Description
Disposable 3cc Syringe LL, W/BioGuard Safety Needle 21G x 1" FDA UDI

Identifiers

Catalog Number
BIO-1051S FDA UDI
Primary DI / UDI-DI
00858835007103 FDA UDI
510(k) Number
K112057 FDA UDI
K190183 FDA UDI
FDA Product Code
FMF FDA UDI
FMI FDA UDI
MEG FDA UDI
GMDN Term
General-purpose syringe, single-use 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: Hypodermic needle, single-useGeneral-purpose syringe, single-use

Syringe LL, W/BioCare Safety Needle by Biotronix Healthcare Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

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 b2f35fa0-3ce2-4774-a941-5ed280261121 37 fields · synced May 30, 2026