DEVICE: First Aid Only (00092265911313)

Device Identifier (DI) Information

First Aid Only
91131
In Commercial Distribution
91131
Acme United Corporation
00092265911313
GS1

1
001180207 *Terms of Use
SmartCompliance RetroFit Business First Aid, 50 Person - Contains: Alcohol Pads 20 ct; Antibiotic Ointment Packets, 30 ct; Antiseptic Wipes, 30 ct; Burn Dressing, 4" x 4", 2 ct; Burn Relief Packets 6 ct; Conforming Gauze Roll, 2", and 1/2" x 5 yards tape roll; Conforming Gauze Roll, 2"; Conforming Gauze Roll, 4"; CPR Face Shield; Eye Wash, 4 oz.; Fabric Bandages, 1" x 3", 50 ct; First Aid Burn Cream Packets, 20 ct; First Aid Guide; Hand Sanitizer Packets, 10 ct; Instant Cold Pack, 4" x 5" 2 ct; Moleskin Blister Prevention Pads, 2"x 2"; 10 ct; Nitrile Exam Gloves, 8 ct; Padded Splint, 4" x 24"; Scissors; Sterile Eye Pads 2, 1 oz. eyewash and 1/2" x 5 yards tape roll; Sterile Gauze Pads, 3" x 3", 10 ct; Stretch Tourniquet, 1" x 18"; Trauma Pads, 5" x 9", 4 ct; Triangular Bandage, 40" x 40" x 56", 2 ct.
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
No
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

96aa8cb6-1bca-41c5-b6e5-bbb6fccb5a8a
April 15, 2021
2
September 18, 2020
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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
No Package DIs found
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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

[?]
No
No
No
No
No CLOSE

Customer Contact

[?]
800-835-2263
customerservice@acmeunited.com
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