Primary Device ID | 00810477025556 |
NIH Device Record Key | 73cd28c2-728a-47ea-b0ba-02a0be8f0a1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AMPLIM |
Version Model Number | XA205 |
Company DUNS | 080521945 |
Company Name | AMPLIM, 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 | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00810477025556 [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 | 2023-06-05 |
Device Publish Date | 2023-05-28 |
00810477025501 | XA201 |
00810477025587 | XA208 |
00810477025570 | XA207 |
00810477025563 | XA206 |
00810477025556 | XA205 |
00810477025532 | XA204 |
00810477025525 | XA203 |
00810477025518 | XA202 |
00810477026232 | A8175-15-DV |
00810477026225 | A8173-10-DV |
00810477026218 | A8172-6-DV |
00810477026201 | A8171-3-DV |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMPLIM 97977076 not registered Live/Pending |
Amplim, LLC 2022-04-13 |
AMPLIM 97362279 not registered Live/Pending |
Amplim, LLC 2022-04-13 |
AMPLIM 87812678 5575552 Live/Registered |
Amplim LLC 2018-02-27 |
AMPLIM 86119246 4555929 Live/Registered |
Amplim, LLC 2013-11-14 |