Primary Device ID | 00850052737009 |
NIH Device Record Key | 91c26827-c1b1-4a83-bd3f-710ff0b32425 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sea-Long Medical Hood |
Version Model Number | 500 Seris Model |
Company DUNS | 622106151 |
Company Name | Sea-Long Medical Systems 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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com | |
Phone | +1(502)969-4949 |
melissa@sea-long.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850052737009 [Primary] |
FOG | HOOD, OXYGEN, INFANT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
[00850052737009]
Ultraviolet Light
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-29 |
Device Publish Date | 2024-11-21 |