NUK® Single Electric Breast Pump 91003192

GUDID 20885131627661

NUK USA LLC

Breast pump, electric

• Primary Device ID: 20885131627661
• NIH Device Record Key: 04abc891-33ff-4408-a112-19c574f0d481
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NUK® Single Electric Breast Pump
• Version Model Number: 62766
• Catalog Number: 91003192
• Company DUNS: 830201237
• Company Name: NUK USA LLC
• 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: 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	00885131627667 [Primary]
GS1	20885131627661 [Package]; Contains: 00885131627667; Package: Corrugate Box [2 Units]; In Commercial Distribution

FDA Product Code

• HGX: Pump, Breast, Powered

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: 2018-03-29
• Device Publish Date: 2016-04-29

Devices Manufactured by NUK USA LLC

• 10885131760873 - first essentials Nasal Aspirator: 2019-05-17
• 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
• 20885131627661 - NUK® Single Electric Breast Pump: 2018-03-29