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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 Syringe 1 mL, Luer Lock, Standard Plunger, Sterile FDA UDI
Model / Reference
RM-403001 FDA UDI
Description
Ceros Syringe 1 mL, Luer Lock, Standard Plunger, Sterile FDA UDI

Identifiers

Catalog Number
RM-403001 FDA UDI
Primary DI / UDI-DI
00850060997785 FDA UDI
510(k) Number
K210200 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 — 1 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.

Cleared under the same submission

K210200 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4cbba8de-28b5-4872-b10a-5a815ba99d6f 37 fields · synced Jun 1, 2026