DEVICE: Ozark Trail Outdoor Equipment (00017276235869)
Device Identifier (DI) Information
Ozark Trail Outdoor Equipment
017276235869
Not in Commercial Distribution
WAL-MART STORES, INC.
017276235869
Not in Commercial Distribution
WAL-MART STORES, INC.
All-Purpose First Aid Kit, 205 items: 40 - Antibacterial Sheer Bandages 7/8 IN (22 mm); 30 - Antibacterial Sheer Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 30 - Antibacterial Fabric Bandages 5/8 IN x 2 1/4 IN (15 mm x 57 mm); 20 - Antibacterial Fabric Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 14 - Butterfly Closures 1 3/4 IN x 3/8 IN (44 mm x 9 mm); 20 – Alcohol Prep Pads 1 3/16 IN x 2 5/16 IN (30 mm x 58 mm); 8 - Acetaminophen (2 tablets per packet); 5 - Hydrocortisone Cream 1/32 OZ (0.9 g); 4 – Diphen Allergy Caplets (1 caplet per packet); 3 - Antiseptic Wipes 4 3/4 IN x 7 3/4 IN (120 mm x 196 mm); 2 – Triple Antibiotic Ointments 1/32 OZ (0.9 g); 2 - Topical Cooling Gel 1/8 OZ (3.5 g); 1 – First Aid & Burn Cream 1/32 OZ (0.9 g); 1 - Sunscreen Lotion SPF 30 1/8 OZ (3.5 g); 4 – Wooden Finger Splints; 2 - Cotton Tipped Applicators 3 IN (76 mm) 2 per packet; 2 - Nitrile Gloves; 1 - Single use instant Cold Pack; 1 - Pair of Tweezers; 1 - Paper Tape 1/2 IN x 5 YDS (12.7 mm x 4.5 m); 1 - First Aid Guide; 6 - Gauze Pads 2 IN x 2 IN (50 mm x 50 mm); 3 - Non-Stick Pads 2 IN x 3 IN (50 mm x 76 mm); 1 - Gauze Pad 4 IN x 4 IN (101 mm x 101 mm); 1 - Hydrogel Burn Pad 1.96 IN x 2.96 IN (49 mm x 74 mm); 1 - Rolled Gauze 2 IN x 2.5 YDS (50 mm x 2.28 m); 1 - Carrying case
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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44039 | First aid kit, medicated |
A convenient collection of equipment, materials and pharmaceuticals intended to be used in an emergency for the rapid, initial treatment of an injury. It is typically used by emergency medical services (EMS), hospitals, institutions, schools, and other public settings. This is a reusable device.
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FDA Product Code
[?]Product Code | Product Code Name |
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LRR | First Aid Kit With Drug |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
7ddfdbbf-7c70-4220-b57a-6ebfa3679059
August 19, 2021
2
December 09, 2019
August 19, 2021
2
December 09, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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20017276235863 | 2 | 00017276235869 | 2021-01-26 | Not in Commercial Distribution | case |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined