Primary Device ID | B24523001B1 |
NIH Device Record Key | 4e62dbca-30ff-40c2-b2b7-9939d9cbe8c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SSCOR/board |
Version Model Number | 23001B |
Company DUNS | 131254971 |
Company Name | SSCOR, INC. |
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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B24523001B1 [Primary] |
GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-23 |
Device Publish Date | 2016-09-16 |
B245250001 | Onboard Suction Device |
B24523001WCKK1 | Onboard Suction Device |
B24523001WCK15 | Onboard Suction Device |
B24523001WC1 | Onboard Suction Device |
B24523001PLC1 | Onboard Suction Device |
B24523001B1 | Onboard Suction Device |
B245230011 | Onboard Suction Device |
B245225001 | Onboard Suction Device |
B24522020LDR12 | Onboard Suction Device |
B24522000RRC15 | Onboard Suction Device |
B24522000PLC1 | Onboard Suction Device |
B24522000GIFA1 | Onboard Suction Device |
B24522000BRAUN1 | Onboard Suction Device |
B245220001 | Onboard Suction Device |