Primary Device ID | 43661234025235 |
NIH Device Record Key | 89a8631d-121c-418a-9fc7-9d28fbe9b928 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PEROUSE MEDICAL |
Version Model Number | E63101EA |
Catalog Number | VPEE63101EA |
Company DUNS | 267476323 |
Company Name | PEROUSE MEDICAL |
Device Count | 2 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03661234025237 [Primary] |
GS1 | 33661234025238 [Package] Package: [1 Units] In Commercial Distribution |
GS1 | 43661234025235 [Package] Contains: 03661234025237 Package: [5 Units] In Commercial Distribution |
GS1 | 63661234025239 [Unit of Use] |
GDF | GUIDE, NEEDLE, 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 | 2024-04-03 |
Device Publish Date | 2024-03-26 |
33661234025269 | NEEDLE GUIDE Ø2,25MM |
33661234025252 | NEEDLE GUIDE Ø1,2MM |
33661234025245 | NEEDLE GUIDE Ø1,0MM |
43661234025228 | NEEDLE GUIDE Ø1,8MM |
33661234025184 | NEEDLE GUIDE Ø0,9MM |
43661234025235 | NEEDLE GUIDE Ø0,9MM |
43661234025198 | NEEDLE GUIDE Ø1,0MM |
33661234025207 | NEEDLE GUIDE Ø1,2MM |
33661234025214 | NEEDLE GUIDE Ø1,4MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PEROUSE MEDICAL 79076547 3916165 Live/Registered |
PEROUSE MEDICAL 2009-09-04 |
PEROUSE MEDICAL 79075995 3916156 Live/Registered |
PEROUSE MEDICAL 2009-09-04 |