RAPID RESPONSE EMERGENCY KIT

GUDID 10850015055598

4.25" X 24" FLEX PADDED SPLINT ARC FIRST AID GUIDE ANSI 2021 NITRILE EXAM GLOVES 2/BAG ANSI TRIANGULAR BDG 1/BAG COLD PACK 4X5 BULK CPR FACE SHIELD W/1-WAY VALVE 3X3" STERILE GAUZE PAD (2 PACK) WINDLASS TOURNIQUET NUSTAT HEMOSTATIC GAUZE PAD 4"X4" HEMA-SEAL 8X10 COMPRESSED TRAUMA DRESSING BULK 5"X9" COMBINE DRESSING BULK TOURNIQUET BULK 1"X18" 1/2" X 5YD ADHESIVE TAPE BULK STERILE BURN DRESSING 4"X4" BZK WIPES, FAO, 5X7, SINGLE WIPE FIRST AID BURN CREAM PKT 0.9G 4.75" BLACK BANDAGE SHEAR 2" X 4YD NS GAUZE ROLL BULK HAND SANITIZER 0.9GM BULK EYEWASH 4 OZ (SCREW TOP) 4" X 4 YD HS GAZUE ROLL BULK STERILE EYE PAD BULK SANIZIDE PLUS WIPES LG BULK ABSORBENT POWDER 2OZ HEAT SEALED BAG SCOOP/SPATULA PLASTIC BULK NON-SURGICAL GOWNS PAPER TOWELS BULK FACE MASK W/SHIELD BIOHAZARD BAG 24X24 BULK ANTIMICROBIAL WIPES "PAWS" BAG PLASTIC 10X12" RECLOSABLE TWIST TIES (GREEN) ALCOHOL PREP PAD, FAO, SOLDIER, STERILE NEOMYCIN ANTIBIOTIC OINTMENT 0.9G BULK BANDAGE PLASTIC 1X3" 5-UP 1X3" FABRIC ADHESIVE BANDAGES 5-UP EMERGENCY BLANKET

ULINE, INC.

First aid kit, medicated

• Primary Device ID: 10850015055598
• NIH Device Record Key: a250d43f-228c-460e-b0ea-62d3f5ac00de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAPID RESPONSE EMERGENCY KIT
• Version Model Number: H-11044
• Company DUNS: 039612668
• Company Name: ULINE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: true
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	10850015055598 [Primary]

FDA Product Code

• LRR: First Aid Kit With Drug

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-06
• Device Publish Date: 2024-01-29

Devices Manufactured by ULINE, INC.

• 30850015055509 - ULINE REUSABLE EARPLUGS - UNCORDED: 2024-08-02
• 30850015055516 - ULINE REUSABLE EARPLUGS - CORDED: 2024-08-02
• 30850015055523 - ULINE BULLET EARPLUGS - UNCORDED: 2024-07-31
• 30850015055530 - ULINE BULLET EARPLUGS - CORDED: 2024-07-31
• 30850015055547 - ULINE BELL EARPLUGS - UNCORDED: 2024-07-31
• 30850015055554 - ULINE BELL EARPLUGS - CORDED: 2024-07-31
• 30850015055493 - ULINE BULLET EARPLUGS REFILL: 2024-05-21
• 00850015055713 - ULINE EARPLUGS IN A BUCKET: 2024-05-21