ANSI First Aid Kit Class B+, 250 Person

GUDID 10850015055321

(4) ABSORBENT COMPRESS, (25) ANTACID, (50) ANTIBIOTIC OINTMENT, (54) ANTISEPTIC TOWELETTE, (25) ASPIRIN, (2) BURN DRESSING, (1) COHESIVE ELASTIC BANDAGE, (100) COTTON SWAB, (75) COUGH DROPS, (2) CPROTECTOR, (25) EXTRA-STRENGTH ACETAMINOPHEN, (16) EYE PAD WITH TAPE, (25) FABRIC FINGERTIP BANDAGE, (25) FABRIC KNUCKLE BANDAGE, (50) BURN CREAM, (1) FIRST AID FACTS GUIDE, (3) FIRST AID TAPE, (25) GAUZE PAD, (4) 2" X 6 YD GAUZE ROLL, (2) 4" X 6 YD GAUZE ROLL, (23) HAND SANITIZER, (25) IBUPROFEN, (2) INSTANT ICE PACK, (4) NITRILE GLOVE 1, (25) NON-STICK PAD, (100) PLASTIC BANDAGE, (1) PLASTIC TWEEZERS, (1) SAM SPLINT, (1) SCISSORS, (1) SINGLE USE SALINE, (10) STING WIPES, (1) TOURNIQUET, (1) TRAUMA DRESSING, (3) TRIANGULAR BANDAGE, (1) TOPICAL POWDER, (50) 3/4" X 3" PLASTIC BANDAGE, (25) 2" X 3" PLASTIC BANDAGE, (50) FABRIC BANDAGE, (1) EMERGENCY RESCUE BLANKET, (1) ABSORBENT POWDER, (1) BAG WITH SCOOP, (1) BIOHAZARD BAG, (1) DISPOSABLE FACE MASK WITH SHIELD, (2) GERMICIDAL WIPE, (1) INFECTION CONTROL GOWN, (2) NITRILE GLOVE 2, (2) PAPER TOWEL, (1) PLEATED BOUFFANT

ULINE, INC.

First aid kit, medicated

• Primary Device ID: 10850015055321
• NIH Device Record Key: 3d19f601-aa2a-48a7-a5f3-c6625768b114
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANSI First Aid Kit Class B+, 250 Person
• Version Model Number: H-9997
• Company DUNS: 039612668
• Company Name: ULINE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	10850015055321 [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: 2022-03-30
• Device Publish Date: 2022-03-22

Devices Manufactured by ULINE, INC.

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• 30850015055578 - ULINE EXAM GRADE NITRILE GLOVES - POWDER-FREE, MEDIUM: 2025-05-06
• 30850015055585 - ULINE EXAM GRADE NITRILE GLOVES - POWDER-FREE, SMALL: 2025-05-06
• 30850015055592 - ULINE EXAM GRADE NITRILE GLOVES - POWDER-FREE, XL: 2025-05-06
• 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