NUK® Manual Breast Pump 91002243

GUDID 00885131627735

NUK USA LLC

Breast pump, manual

• Primary Device ID: 00885131627735
• NIH Device Record Key: 2619ec91-6079-4d0a-9204-8ff37b48aa2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NUK® Manual Breast Pump
• Version Model Number: 62773
• Catalog Number: 91002243
• Company DUNS: 830201237
• Company Name: NUK USA LLC
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885131627735 [Primary]

FDA Product Code

• HGY: Pump, Breast, Non-Powered

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: 2018-04-23
• Device Publish Date: 2018-03-21

Devices Manufactured by NUK USA LLC

• 10885131760873 - first essentials Nasal Aspirator: 2019-05-17
• 00885131627735 - NUK® Manual Breast Pump: 2018-04-23
• 00885131627735 - NUK® Manual Breast Pump: 2018-04-23
• 10885131626018 - NUK® Double Electric Breast Pump: 2018-03-29
• 20885131627661 - NUK® Single Electric Breast Pump: 2018-03-29