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ReddyPort

FDA UDI

Class I (US FDA UDI)

by Smd Manufacturing Llc

Identity

Trade Name
ReddyPort FDA UDI
Generic Name
Cannulated manual toothbrush FDA UDI
Device Name
ReddyPort 24-hour NIV Maintenance Kit follows Q4 protocols (every 4 hours) for standard oral care procedures. FDA UDI
Model / Reference
RP-MKITQ4-2 FDA UDI
Description
ReddyPort 24-hour NIV Maintenance Kit follows Q4 protocols (every 4 hours) for standard oral care procedures. FDA UDI

Identifiers

Primary DI / UDI-DI
00850001175227 FDA UDI
FDA Product Code
KXF FDA UDI
JOL FDA UDI
EFW FDA UDI
GMDN Term
Cannulated manual toothbrush FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 FDA UDI
880.6740 FDA UDI
872.6855 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

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: Cannulated manual toothbrush

ReddyPort by Smd Manufacturing Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated manual toothbrush.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smd Manufacturing Llc

Sources (1)

  • FDA UDI d54461e7-ed19-4c3c-ada4-8e0e4b732c3e 35 fields · synced May 30, 2026