Adventure Medical Kits - Adventure First Aid, 2.0Medical Information1 - - Adventure Ready Brands

Duns Number:064437304

Device Description: Adventure First Aid, 2.0Medical Information1 - Easy Care First Aid & Survival Instructions Adventure First Aid, 2.0Medical Information1 - Easy Care First Aid & Survival InstructionsSurvival Tools1 - Slim Rescue Howler™ Whistle1 - Compass, Button, Liquid FilledBandage Materials12 - Antiseptic Wound Wipe4 - Bandage, Butterfly Closure16 - Bandage, Adhesive, Fabric, 1" x 3"1 - Bandage, Adhesive, Fabric, 2" x 4.5"4 - Bandage, Adhesive, Fabric, Knuckle4 - Dressing, Gauze, Sterile, 4" x 4", 2 Pkg./24 - Dressing, Gauze, Sterile, 2" x 2", 2 Pkg./24 - Dressing, Gauze, Sterile, 3" x 3", 2 Pkg./22 - Dressing, Non-Adherent, Sterile, 2" x 3", 2 Pkg./14 - Cotton Tip ApplicatorBleeding1 - Gloves, Nitrile (Pair), Hand Wipe1 - Sterile Pad, 5" x 9"Blister / Burn1 - Moleskin, Pre-Cut & Shaped (11 pieces)Sprain / Strain1 - Bandage, Elastic with Clips, 2"1 - Instant Cold PackInstrument2 - Safety Pins1 - Scissors, Bandage with Blunt Tip1 - Splinter Picker/Tick Remover ForcepsMedication6 - Acetaminophen (500 mg), 3 Pkg./23 - Antihistamine (Diphenhydramine 25 mg) 3 Pkg./16 - Ibuprofen (200 mg), 3 Pkg./21 - Aspirin (325 mg), 1 Pkg./2Other1 - After Bite® Insect ReliefWound Care12 - Antiseptic Wipe2 - Cotton Tip Applicator, Pkg./21 - Tape, 1/2" x 10 Yards4 - Triple Antibiotic Ointment, Single Use

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More Product Details

Catalog Number

0120-0220

Brand Name

Adventure Medical Kits

Version/Model Number

1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

LRR

Product Code Name

First Aid Kit With Drug

Device Record Status

Public Device Record Key

34bf2e00-16a4-4170-83ad-718edf5854be

Public Version Date

September 17, 2020

Public Version Number

2

DI Record Publish Date

December 27, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-