Primary Device ID | 03661219199229 |
NIH Device Record Key | 3f74aabd-6744-4f8d-b204-0e05dd041e19 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LANDANGER |
Version Model Number | B607571 |
Company DUNS | 299889175 |
Company Name | LANDANGER |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03661219199229 [Primary] |
DWS | Instruments, Surgical, Cardiovascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
[03661219199229]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-12 |
Device Publish Date | 2024-09-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LANDANGER 73652566 1480581 Dead/Expired |
LANDANGER (S.A.) 1987-04-01 |