Primary Device ID | 03661522000984 |
NIH Device Record Key | 4de2a67e-d27f-4295-ac04-93a4af25118c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sertilac |
Version Model Number | 32300M20 |
Company DUNS | 265741780 |
Company Name | PETERS SURGICAL |
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 | true |
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 | 03661522000984 [Primary] |
GAE | Snare, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-19 |
Device Publish Date | 2023-06-09 |
03661522100882 - Applier, hemostatic clip | 2024-01-10 |
03661522100899 - Applier, hemostatic clip | 2024-01-10 |
03661522100905 - Applier, hemostatic clip | 2024-01-10 |
03661522100929 - Applier, hemostatic clip | 2024-01-10 |
03661522100936 - Applier, hemostatic clip | 2024-01-10 |
03661522100912 - Applier, hemostatic clip | 2024-01-05 |
03661522000984 - Sertilac | 2023-06-19 |
03661522000984 - Sertilac | 2023-06-19 |
03661522039540 - Applier, hemostatic clip | 2023-06-16 |