Duns Number:086911794
Device Description: 4-Shelf Kit Fill1- Adhesive Bandage 1” x 3” Strip, 100/box1- Adhesive Bandage, 7/8” x 3” S 4-Shelf Kit Fill1- Adhesive Bandage 1” x 3” Strip, 100/box1- Adhesive Bandage, 7/8” x 3” Strip, 50/box1- Adhesive Bandage, Fingertip, 40/box1- Adhesive Bandage, Knuckle, 40/box1- Adhesive Tape, Tri-Cut 5yd1- Alcohol Prep Pads, 50/box1- Ammonia Wipes, 10/box1- Antacid Tablets, 250/box1- Antiseptic Spray 2oz Pump1- Antiseptic Wipes-XL, 20/box1- Bloodstopper Compress 9” x 5”1- Burn Gel Unit Dose 1/8oz pkt2- Burn Dressing 4” x 4”1- Burn Spray 2oz Pump2- Cold Pack, Small, Boxed1- Cold Relief Tablets, 100/box2- Cotton Tip 3” Applicator, 10/bag1- CPR Mask/Breathing Barrier1- Medicated Eye Drops, 0.5oz4- Eye Pads1- Eyewash 4oz1- First Aid Handbook1- Gauze Pad 3” x 3”, Sterile, 25/box2- Gauze Roll 2” x 5yds1- Gauze Roll 4” x 5yds1- Hand Sanitizer, 10/bag10- Non-Adherent Sterile Pads 2” x 3” Sterile1- Non-Aspirin Tablets, 100/box1- Pain Relief Tablets, 250/box4-- Powder Free Exam Gloves, Disposable, Pair/L1- Self-Adherent Wrap 2”1- Scissors 4.5”1- Splint, Multi-Purpose1- Thera-Tears1- Tourniquet4- Trauma Pads 5” x 9”2- Triangular Bandage with Pins, Non-Sterile1- Triple Antibiotic Ointment, 25/box1- Tweezers, Plastic, Disposable
Catalog Number
703ANSI
Brand Name
Medi-First 4-Shelf ANSI First Aid Cabinet
Version/Model Number
703ANSI
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
LRR
Product Code Name
First Aid Kit With Drug
Public Device Record Key
9a6cab72-1412-4d2b-a993-f3d0c65226b8
Public Version Date
November 06, 2019
Public Version Number
1
DI Record Publish Date
October 29, 2019
Package DI Number
50347682703245
Quantity per Package
1
Contains DI Package
00347682703240
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
master case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 110 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1 |
| U | Unclassified | 1 |