Primary Device ID | 14063108108675 |
NIH Device Record Key | 49aeece1-00d1-4922-a214-340b697ece5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SURVAC™ |
Version Model Number | 77642SC |
Company DUNS | 777211640 |
Company Name | NOVATECH |
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 | 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 | 14063108108675 [Primary] |
BSY | Catheters, Suction, Tracheobronchial |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-26 |
Device Publish Date | 2024-06-18 |
14063108108675 | Suction Catheters for Bronchoscopy PC, 3 x 4, L 30 |
14063108108668 | Suction Catheters for Bronchoscopy PC, 3 x 4, L 60 |
14063108108651 | Suction Catheters for Bronchoscopy PC, 2 x 2.7, L 60 |
14063108108644 | Suction Catheters for Bronchoscopy PTFE, 2 x 3, L 60 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURVAC 79064459 3712295 Dead/Cancelled |
Merck KGaA 2008-12-19 |