Primary Device ID | 00810104130950 |
NIH Device Record Key | 11f55b53-2f56-49a3-a166-8b530d1131aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wave, Container 5oz, Replacement |
Version Model Number | RC0511 |
Company DUNS | 050917861 |
Company Name | WILLOW INNOVATIONS, 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00810104130950 [Primary] |
HGY | Pump, Breast, Non-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-31 |
Device Publish Date | 2025-07-23 |
00810104130936 - Wave Single Manual Pump Kit | 2025-07-31 |
00810104130943 - Willow Sync, Pump Kit | 2025-07-31 |
00810104130950 - Wave, Container 5oz, Replacement | 2025-07-31 |
00810104130950 - Wave, Container 5oz, Replacement | 2025-07-31 |
00810104130967 - Wave, Gasket, 2 pack, Retail | 2025-07-31 |
00810104130974 - Wave, Flapper Valves, 4 pack, Retail | 2025-07-31 |
00810104130981 - Wave, Flange 24mm, Replacement | 2025-07-31 |
00810104130998 - Wave, Single, Tubing Set, Retail | 2025-07-31 |
00810104131001 - Wave, Handle, Replacement | 2025-07-31 |