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Ceros

FDA UDI

Class II (US FDA UDI)

by Rhino Medical Supply Inc

Identity

Trade Name
Ceros FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
Ceros Safety Hypodermic Needle and Syringe Combo, 3 mL 20 G x 1 1/2" Yellow Luer Lock Tip Hub, Latex Free, DEHP Free, PVC Free FDA UDI
Model / Reference
RM-SNO132015LS FDA UDI
Description
Ceros Safety Hypodermic Needle and Syringe Combo, 3 mL 20 G x 1 1/2" Yellow Luer Lock Tip Hub, Latex Free, DEHP Free, PVC Free FDA UDI

Identifiers

Catalog Number
RM-SNO132015LS FDA UDI
Primary DI / UDI-DI
00850060997778 FDA UDI
510(k) Number
K193526 FDA UDI
FDA Product Code
FMI FDA UDI
MEG FDA UDI
FMF FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
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

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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI
Needle Gauge — 20 Gauge FDA UDI
Length — 1.5 Inch FDA UDI

Category: General-purpose syringe/needle

Ceros by Rhino Medical Supply Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe/needle.

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 23db0889-478f-4234-9a19-b333b955e3ae 37 fields · synced Jun 6, 2026