Primary Device ID | 03700393300196 |
NIH Device Record Key | 9a4a07dd-b5ed-4b50-a4fd-a33d361bc8d6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5068 |
Catalog Number | 5068 |
Company DUNS | 265741780 |
Company Name | PETERS SURGICAL |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com | |
Phone | +1 508-747-6033 |
e.knupp@peters-surgical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700393300196 [Package] Contains: 03700393300202 Package: Box [25 Units] In Commercial Distribution |
GS1 | 03700393300202 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2016-09-12 |
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 |
03661522039540 - Applier, hemostatic clip | 2023-06-16 |