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 Hypodermic Needle & Syringe Combo, 5 mL, 21 G x 1", Detachable, Green Polypropylene Hub, Latex Free, DEHP Free, PVC Free FDA UDI
Model / Reference: RM-SN0152110D FDA UDI
Description: Ceros Hypodermic Needle & Syringe Combo, 5 mL, 21 G x 1", Detachable, Green Polypropylene Hub, Latex Free, DEHP Free, PVC Free FDA UDI

Identifiers

Catalog Number: RM-SN0152110D FDA UDI
Primary DI / UDI-DI: 00850041572932 FDA UDI
FDA Product Code: FMF FDA UDI
FMI FDA UDI
GMDN Term: General-purpose syringe/needle 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Total Volume — 5 Milliliter FDA UDI
Needle Gauge — 21 Gauge FDA UDI
Length — 1 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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Rhino Medical Supply Inc

Sources (1)

FDA UDI 086960a8-e153-43b6-b062-f1717a8379e7 36 fields · synced May 31, 2026