Primary Device ID | 00785811435738 |
NIH Device Record Key | f89d8b9b-5963-4a90-8f03-5d0a639a8347 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boston IV |
Version Model Number | itafocon B |
Catalog Number | Boston IV |
Company DUNS | 058816302 |
Company Name | BAUSCH & LOMB INCORPORATED |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00785811435738 [Primary] |
HQD | Lens, Contact (Other Material) - Daily |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-12-13 |
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