Primary Device ID | 10810038633272 |
NIH Device Record Key | 8916fc55-e831-4b79-a27f-6aa3f934375c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Premom Pregnancy Test Midstream (5 Tests) |
Version Model Number | PMS1-M |
Catalog Number | PM1-M3-5 |
Company DUNS | 080278407 |
Company Name | EASY HEALTHCARE CORPORATION |
Device Count | 5 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00810038633275 [Primary] |
GS1 | 10810038633272 [Package] Contains: 00810038633275 Package: Carton [96 Units] In Commercial Distribution |
GS1 | 30810038633276 [Unit of Use] |
LCX | Kit, Test, Pregnancy, Hcg, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-28 |
Device Publish Date | 2023-04-20 |
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