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Oak Ridge Products

FDA UDI

Class I (US FDA UDI)

by Oak Ridge Products

Identity

Trade Name
Oak Ridge Products FDA UDI
Generic Name
Medicine cup, single-use FDA UDI
Device Name
30mL Metric Medicine cup, packaged 100 cups/sleeve, 50 sleeves/case, 5,000 Cups Per Case, made of Polypropylene FDA UDI
Model / Reference
0105-0100 FDA UDI
Description
30mL Metric Medicine cup, packaged 100 cups/sleeve, 50 sleeves/case, 5,000 Cups Per Case, made of Polypropylene FDA UDI

Identifiers

Primary DI / UDI-DI
00852482006830 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
Medicine cup, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medicine cup, single-use

Oak Ridge Products by Oak Ridge Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine cup, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oak Ridge Products

Sources (1)

  • FDA UDI c1d65edc-99dc-422a-9d83-eb1bd3313cc9 34 fields · synced May 30, 2026