Harris Teeter

GUDID 10072036722710

AL-BAD MASSUOT YITZHAK LTD

Menstrual pad, unscented Menstrual pad, unscented Menstrual pad, unscented Menstrual pad, unscented

• Primary Device ID: 10072036722710
• NIH Device Record Key: cfebfc96-31fc-4865-be70-00facbac0435
• Commercial Distribution Discontinuation: 2022-05-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Harris Teeter
• Version Model Number: BCNHTSUTS32
• Company DUNS: 600487813
• Company Name: AL-BAD MASSUOT YITZHAK LTD
• Device Count: 32
• 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: 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00072036722713 [Primary]
GS1	00834533001575 [Unit of Use]
GS1	10072036722710 [Package]; Contains: 00072036722713; Package: CASE [6 Units]; Discontinued: 2022-05-01; Not in Commercial Distribution

FDA Product Code

• HHD: Pad, Menstrual, Unscented

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-05-23
• Device Publish Date: 2020-06-01

On-Brand Devices [Harris Teeter]

• 10072036722727: BCNHTSUTR36
• 10072036722710: BCNHTSUTS32
• 10072036722703: BCNHTZPLL54
• 10072036722697: FUSHTSPLL40
• 10072036722680: BCNHTSUTS16
• 10072036722673: BCNHTSUTR18
• 10072036722666: FUSHTZPLL64
• 10072036722659: BCNHTSUTO28
• 10072036722642: BCNHTSUTO14