DEVICE: Care Science (00017276237559)

Device Identifier (DI) Information

Care Science
00017276237559
In Commercial Distribution
B08QDTH131
Aso LLC
00017276237559
GS1

1
152793493 *Terms of Use
On - the - Go, First Aid Kit, 100 pieces: 20 Sheer Bandages 3/4 IN X 3 IN (19 MM X 76 MM); 15 Sheer Bandages 5/8 IN X 2 1/4 IN (15 MM X 57 MM); 5 Butterfly Closures 1 3/4 IN X 3/8 IN (44 MM X 9.5 MM); 2 Fabric Fingertip Bandages 1 3/4 IN X 2 IN (44 MM X 50 MM); 2 Fabric Knuckle Bandages 1 1/2 IN X 3 IN (38 MM X 76 MM); 2 Wooden Finger Splints; 1 Breathing Barrier; 1 First Aid Guide; 1 Instant Cold Pack; 1 Metal Scissors; 1 Metal Tweezers; 1 Paper Tape Roll 1/2 IN X 5 YDS (12.5 MM X 4.5 M); 1 Tender Tape Roll 1 IN X 5 YDS (25 MM X 4.5 M); 1 Triangular Sling 40 IN X 40 IN X 56 IN (101 CM X 101 CM X 142 CM); 10 Alcohol Prep Pads 1 3/16 IN X 2 5/16 IN (30 MM X 58 MM); 10 Triple Antibiotic Ointment 1/32 OZ (0.9 G); 8 Hand Sanitizers 1/32 OZ (0.9 G); 4 Antiseptic Wipes 4 3/4 IN X 7 3/4 IN (120 MM X 196 MM); 6 Blister Cushions 0.67 IN X 2 IN (17 MM X 50 MM); 6 Gauze Pads 2 IN X 2 IN (50 MM X 50 MM); 1 Burn Dressing 4 IN X 4 IN (100 MM X 100 MM); 1 Rolled Gauze 2 IN X 2 1/2 YDS (50 MM X 2.2 M).
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Device Characteristics

Labeling does not contain MRI Safety Information
No
Yes
Yes
No
Yes
Yes
Yes
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?
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.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
LRR First Aid Kit With Drug
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
Yes CLOSE

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

355002ab-3e69-4b43-b5c7-8a6c707f1fa7
May 19, 2021
1
May 11, 2021
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
20017276237553 10 00017276237559 In Commercial Distribution case
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
8558234545
regulatory@asocorp.com
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