Primary Device ID | 20643169175093 |
NIH Device Record Key | 8aa80854-dffc-4be3-99db-78c48917d171 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PlasmaBlade(TM) |
Version Model Number | PS300-004 |
Company DUNS | 030200852 |
Company Name | MEDTRONIC, INC. |
Device Count | 16 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169175099 [Unit of Use] |
GS1 | 20643169175093 [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 | 3 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-05-14 |
00643169617193 | PLASMABLADE PS200-040-SP 4.0 MPSS |
00643169617186 | PLASMABLADE PS200-040 EA 4.0 PINK MPSS |
00643169617179 | PLASMABLADE PS200-040 4.0 MPSS |
00643169617162 | PLASMABLADE PS210-030S-SP LOCK MPSS |
00643169617155 | PLASMABLADE PS210-030S PINK LOCK MPSS |
00643169617148 | PLASMABLADE PS210-030S 3.0S LOCK MPSS |
00643169617131 | PLASMABLADE PS210-030P PLUS LOCK MPSS |
20643169175130 | PLASMABLADE PS300-003 ADENOID 4PK |
20643169175123 | PLASMABLADE PS200-001 4PK NEEDLE |
20643169175116 | PLASMABLADE PS300-002 TNA 4PK |
20643169175109 | PLASMABLADE PS300-001 TONSIL 4PK |
20643169175093 | PLASMABLADE PS300-004 SUCT COAG BLA 16PK |