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Moisturizer

FDA UDI

Class II (US FDA UDI)

by Smd Manufacturing Llc

Identity

Trade Name
Moisturizer FDA UDI
Generic Name
Oral care swab FDA UDI
Device Name
ReddyPort Moisturizer Pack for use with ReddyPort Elbow. Moisturizer Pack includes: 1x suction swab, 1x mouth moisturizer, 1x applicator swab FDA UDI
Model / Reference
RP-MPK-1 FDA UDI
Description
ReddyPort Moisturizer Pack for use with ReddyPort Elbow. Moisturizer Pack includes: 1x suction swab, 1x mouth moisturizer, 1x applicator swab FDA UDI

Identifiers

Primary DI / UDI-DI
00850001175203 FDA UDI
FDA Product Code
JOL FDA UDI
KXF FDA UDI
GMDN Term
Oral care swab FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
880.6025 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oral care swab

Moisturizer by Smd Manufacturing Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral care swab.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0dae8480-c69f-4792-8dd6-2cf4c091e905 33 fields · synced Jun 8, 2026