Home GUDID 10850001175224 ReddyPort
Primary DI 10850001175224
Brand ReddyPort
Company SMD Manufacturing LLC
Model RP-MKITQ4-2
Device description ReddyPort 24-hour NIV Maintenance Kit follows Q4 protocols (every 4 hours) for standard oral care procedures.
Published 2023-07-12
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KXF Applicator, Absorbent Tipped, Non-Sterile
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10850001175224 Package GS1 10 In Commercial Distribution 00850001175227 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 10850001175224 10850001175224 00850001175227 00850001175227 850001175227 0850001175227
GMDN Terms# Term, Definition table Term Definition Cannulated manual toothbrush A non-powered instrument designed to be used by a healthcare provider/caregiver to manually brush clean the teeth and gums of a disabled/geriatric patient while simultaneously removing excess oral fluid (saliva, toothpaste). It consists of a proximal handle with a distal bristle head and an integrated suction cannula. It is intended to be used in conjunction with a suction pump (not included). This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store at Room Temperature
Regulatory Flags# DUNS number 070849038 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit true Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex true Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 10889483563267 BALLARD™ SUNMED, LLC KXF 2026-01-12 10889483563281 BALLARD™ SUNMED, LLC KXF 2026-01-12 10889483563311 BALLARD™ SUNMED, LLC KXF 2026-01-12 10889483563335 BALLARD™ SUNMED, LLC KXF 2026-01-12 10889483563359 BALLARD™ SUNMED, LLC KXF 2026-01-12 07613327680720 Q-Care SAGE PRODUCTS, LLC KXF 2025-12-03 07613327680737 Q-Care SAGE PRODUCTS, LLC KXF 2025-12-03 07613327680744 Q-Care SAGE PRODUCTS, LLC KXF 2025-12-03 07613327680751 Q-Care SAGE PRODUCTS, LLC KXF 2025-12-03 10889483563274 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483563298 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483563328 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483563342 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483565520 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483565537 BALLARD™ SUNMED, LLC KXF 2025-11-17 10889483565544 BALLARD™ SUNMED, LLC KXF 2025-11-17 M220761002 Pro Advantage NATIONAL DISTRIBUTION & CONTRACTING, INC. KXF 2025-09-11 D832600BA4001 MAXAPPLICATOR II PLASDENT CORPORATION KXF 2025-08-01 D832600BF4001 MAXAPPLICATOR II PLASDENT CORPORATION KXF 2025-08-01 10840330701454 ProCure Twin Med, LLC KXF 2024-11-14 10840330701461 ProCure Twin Med, LLC KXF 2024-11-14 10840330701478 ProCure Twin Med, LLC KXF 2024-11-14 10840330701485 ProCure Twin Med, LLC KXF 2024-11-14 00616784430713 "DynaSafety Cotton-Tipped Applicators in Sealed Vial,3""" Dynarex Corporation KXF 2024-11-11 00087701406973 Good Neighbor U.S. COTTON, LLC KXF 2024-07-30 00817522013377 Swabeze KENTEC MEDICAL, INC. KXF 2024-06-28 00817522013353 Swabeze KENTEC MEDICAL, INC. KXF 2024-06-27 00817522013360 Swabeze KENTEC MEDICAL, INC. KXF 2024-06-27 00817522013384 Swabeze KENTEC MEDICAL, INC. KXF 2024-06-27 10817522013343 Swabeze KENTEC MEDICAL, INC. KXF 2024-06-20
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