Primary Device ID | 00730638346095 |
NIH Device Record Key | 7dbe2019-f050-4c0c-93b1-b2c794c8709f |
Commercial Distribution Discontinuation | 2027-12-08 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ann Taylor |
Version Model Number | TYATP91003 |
Company DUNS | 101332278 |
Company Name | L'Amy, Incorporated |
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 | false |
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 | true |
OTC Over-The-Counter | true |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com | |
Phone | 2037610611 |
support@lamyamerica.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00730638346095 [Primary] |
HQY | Sunglasses (Non-Prescription Including Photosensitive) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-12 |
Device Publish Date | 2022-12-02 |