| Primary Device ID | 00858298006552 |
| NIH Device Record Key | a0f489de-df76-4294-92a8-136e06a9e113 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Gen 3 Pump Kit Retail Package, White – 21mm |
| Version Model Number | PDW53 |
| Catalog Number | PDW53 |
| Company DUNS | 050917861 |
| Company Name | EXPLORAMED NC7, INC. |
| 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 | 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 | 00858298006552 [Primary] |
| HGX | Pump, Breast, 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 | 2020-12-23 |
| Device Publish Date | 2020-12-15 |
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| 00810104130714 - Silver Cup | 2024-02-22 Silver Nursing Cup |
| 00810104130707 - Go, Single Pump Kit | 2023-12-18 Go, Single Pump Kit |
| 00810104130462 - 360, Double Pump Kit | 2023-12-15 360, Double Pump Kit |
| 00810104130486 - Double Pump Kit, Willow Go | 2023-04-20 Double Pump Kit, Willow Go (Lucy) |
| 00858298006620 - Willow Go Replacement Pump | 2022-09-08 Willow Go Replacement Pump |
| 00858298006637 - Willow Go Flange Accessory Kit, 21 mm | 2022-09-08 Willow Go Flange Accessory Kit, 21 mm |