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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, single-use FDA UDI
Device Name
Ceros Ring Control Syringe 20 mL, Luer Lock, Sterile Blister Pack, Latex Free, DEHP Free FDA UDI
Model / Reference
RM-03020CON FDA UDI
Description
Ceros Ring Control Syringe 20 mL, Luer Lock, Sterile Blister Pack, Latex Free, DEHP Free FDA UDI

Identifiers

Catalog Number
RM-03020CON FDA UDI
Primary DI / UDI-DI
00850041572109 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe, single-use 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

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 — 20 Milliliter FDA UDI

Category: General-purpose syringe, single-use

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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cbec336-a6c3-4f25-b0d8-a7d0f37d469a 36 fields · synced May 30, 2026