Green Guard Deluxe Vehicle Kit - 1106 -1.000 EACH GG Deluxe Truck Kit Emp 36u6300 - Greenguard

Duns Number:176528040

Device Description: 1106 -1.000 EACH GG Deluxe Truck Kit Emp 36u6300 -1.000 EACH GG 7/8x3 Fabric Strip Bandage 1106 -1.000 EACH GG Deluxe Truck Kit Emp 36u6300 -1.000 EACH GG 7/8x3 Fabric Strip Bandage (50)8205 -1.000 EACH Kit Scissors8203 -1.000 EACH Plastic Single-use Tweezer6112 -1.000 EACH 2" Stretch Roller Gauze NS22312 -1.000 EACH Triple Antibiotic Ointment 10c6102 -1.000 EACH 2" RIP-N-WRAP62612 -1.000 EACH Fingertip Woven M/L 10s62730 -1.000 EACH Woven Knuckle 8s6213 -2.000 EACH 5x9 Combine Dressing ABD60075 -1.000 EACH 1"X3" Plastic Strip 16s6400 -1.000 EACH GG Triangular Bandage +6252 -1.000 EACH Tape 1/2" X 2 1/2 Y3302 -2.000 EACH GG Cold Pack Medium/Boxed +9016B -1.000 EACH First Aid Booklets Ind. for +3004 -1.000 EACH GG Hydrogen Peroxide 2oz pump612B -0.005 M GAUZE 3X3 -7920 -2.000 EACH Glove Wipes21412 -1.000 EACH Antiseptic Towelettes 5X7 10s80201 -1.000 EACH CPR Mask3160 1-.000 EACH WJ Burn Dressing 4x420669 -1.000 EACH Burn Cream w/Lidocaine Unit 4154B -2.000 EACH Large Eye Pads BULK4110 -1.000 EACH GG 1oz Eye Wash17378- 0.006 M Hand Sanitizer BulkANSI-A -1.000 EACH ANSI STICKER A

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More Product Details

Catalog Number

1105

Brand Name

Green Guard Deluxe Vehicle Kit

Version/Model Number

1105

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

e909b960-8867-49c7-ac79-1aed44f26cd5

Public Version Date

July 23, 2019

Public Version Number

1

DI Record Publish Date

July 15, 2019

Additional Identifiers

Package DI Number

50347682110661

Quantity per Package

8

Contains DI Package

00347682110666

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

master case

"GREENGUARD" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 36
2 A medical device with a moderate to high risk that requires special controls. 1
U Unclassified 1