Primary Device ID | 20681490030780 |
NIH Device Record Key | eb90da17-a45b-4a08-8a9b-f092af49f622 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pope Activent® |
Version Model Number | 1035004 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490030786 [Primary] |
GS1 | 20681490030780 [Package] Contains: 00681490030786 Package: PK [5 Units] In Commercial Distribution |
ETD | TUBE, TYMPANOSTOMY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-07-13 |
00763000309480 - Causse/Polycel | 2025-07-01 PROSTHESIS 1156376 CAUSSE FLPL PARTIAL |
20763000870359 - Microgel | 2025-07-01 VENT TUBE 1082201 5PK PAPA TYPE 1.14 |
20763000870366 - Sheehy | 2025-07-01 VENT TUBE 1083301 5PK SHEEHY TYPE 1.27 |
20763000870373 - 20763000870373 | 2025-07-01 VENT TUBE 1084401 5PK GROMMET 1.27 |
20763000870380 - Reuter | 2025-07-01 VENT TUBE 1010201 5PK BOBBIN 1.14 FLPL |
20763000870403 - Sheehy | 2025-07-01 VENT TUBE 1013301 5PK BUTTON 1.27 FLPL |
20763000870410 - Donaldson | 2025-07-01 VENT TUBE 1015101 5PK DONLDSN 1.14 FLPL |
20763000870427 - Shepard | 2025-07-01 VENT TUBE 1016101 5PK GROMMET 1.14 FLPL |