Hyh

GUDID 20885632403764

PRIMARY DRESSING SECONDARY WOUND CARE STERILE SQUARE SILICONE BEIGE MULTI-LAYER CA/50 NOT MADE WITH NaTURAL RUBBER LATEX HYH

OWENS & MINOR DISTRIBUTION, INC.

Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 20885632403764
• NIH Device Record Key: 0d14cddf-2668-4c44-a2f6-d5079e33923c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hyh
• Version Model Number: 50089
• Company DUNS: 007941230
• Company Name: OWENS & MINOR DISTRIBUTION, 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885632403767 [Primary]
GS1	20885632403764 [Package]; Contains: 30885632403761; Package: [5 Units]; In Commercial Distribution
GS1	30885632403761 [Package]; Contains: 10885632403767; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• NAD: Dressing, wound, occlusive

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-26
• Device Publish Date: 2024-06-18

On-Brand Devices [Hyh]

• 20885632407618: Foam Positioner Leg Polyurethane Foam Blue CA/4 31inL x 12inW x 13inH Not made with Natural Rub
• 20885632407601: Foam Positioner Leg Polyurethane Foam Blue CA/3 27inL x 12inW x 15inH Not made with Natural Rub
• 20885632403788: PRIMARY DRESSING SECONDARY WOUND CARE STERILE RECTANGLE SILICONE BEIGE MULTI-LAYER CA/50 NOT MA
• 20885632403764: PRIMARY DRESSING SECONDARY WOUND CARE STERILE SQUARE SILICONE BEIGE MULTI-LAYER CA/50 NOT MADE
• 20885632403757: PRIMARY DRESSING SECONDARY WOUND CARE ICU STERILE SACRAL SILICONE BEIGE MULTI-LAYER CA/25 SACRAL
• 30885632403747: PRIMARY DRESSING SECONDARY WOUND CARE ICU STERILE SACRAL SILICONE BEIGE MULTI-LAYER CA/40 SACRAL
• 20885632403733: PRIMARY DRESSING SECONDARY WOUND CARE STERILE SQUARE SILICONE BEIGE MULTI-LAYER CA/100 NOT MADE
• 20885632403726: PRIMARY DRESSING SECONDARY WOUND CARE STERILE SQUARE SILICONE BEIGE MULTI-LAYER CA/100 NOT MADE
• 20885632403719: PRIMARY DRESSING SECONDARY WOUND CARE STERILE SQUARE SILICONE BEIGE MULTI-LAYER CA/100 NOT MADE