up&up

Primary DI
00017276239614
Brand
up&up
Company
TARGET CORPORATION
Model
245074943
Device description
First Aid Kit, 85 assorted first aid supplies, including one carrying case: 24 Sheer Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 24 Sheer Bandages 5/8 IN x 2 1/4 IN (15 mm x 57 mm); 10 Butterfly Closures 1 3/4 IN x 3/8 IN (44 mm x 9 mm); 3 Fabric Bandages 2 IN x 4 IN (50 mm x 101 mm); 4 - Sterile Pads 2 IN x 2 IN (50 mm x 50 mm); 2 Triple Antibiotic Ointment 0.03 oz (0.9 g); 4 Hand Cleansing Wipes 4 3/4 IN x 7 3/4 IN (120 mm x 196 mm); 6 Alcohol Prep Pad 1 3/16 IN x 2 5/16 IN (30 mm x 58 mm); 2 - Vinyl Gloves; 2 Wooden Finger Splints; 1 - Single Use Instant Cold Pack; 1 - Paper Tape 1/2 IN x 5 YD (12 mm x 4.5 m); - 1 Non-stick Pads 2 IN x 3 IN (50 mm x 76 mm)
Published
2024-02-05
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LRRFirst Aid Kit With Drug

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LRRFirst Aid Kit With DrugUnknownN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20017276239618PackageGS124In Commercial Distribution
00017276239614PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2001727623961820017276239618
00017276239614000172762396140172762396140017276239614

GMDN Terms#

Term, Definition table
TermDefinition
First aid kit, medicatedA 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.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
18558234545xx@xx.xx

Regulatory Flags#

DUNS number
006961700
Device count
1
Premarket exempt
true
Kit
true
Combination product
true
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

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00017276231625Up&Up2450706522020-03-30
00017276233094Up&Up2450705762020-02-28
00017276238655Up&Up2450778132022-02-14
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06941937216819Up & Up245-07-02932022-07-12
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06945397906228Up&Up245-07-07092024-03-01
06945397906242Up&Up245-07-05902024-03-01

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Primary DI, Brand, Company table
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