Primary Device ID | 10814716020811 |
NIH Device Record Key | ad9e0725-623b-497f-a3a7-a985bccee06d |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SFS-300 |
Company DUNS | 809254670 |
Company Name | COASTAL LIFE TECHNOLOGIES, 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 | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814716020814 [Primary] |
GS1 | 10814716020811 [Package] Contains: 00814716020814 Package: [3 Units] In Commercial Distribution |
FYD | Apparatus, Exhaust, Surgical |
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 | 2016-09-23 |
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