Primary Device ID | 00643169103504 |
NIH Device Record Key | a39f0fb5-1f5a-407a-ab1b-63b43726624c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MurphyScope |
Version Model Number | 2125-158 |
Company DUNS | 089055867 |
Company Name | MEDTRONIC PS MEDICAL, INC. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Length | 16 Centimeter |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169103504 [Primary] |
GWG | ENDOSCOPE, NEUROLOGICAL |
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 | 2016-06-13 |
00643169103542 | MURPHYSCOPE 2125-164 MALLE 5 STIP L |
00643169103535 | MURPHYSCOPE 2125-163 MALLE 5 STIP S |
00643169103528 | MURPHYSCOPE 2125-162 MALLE 5 STIP L |
00643169103511 | MURPHYSCOPE 2125-161 CURV MALLE 5 STIP S |
00643169103504 | BAYONET 2125-158 MURPHY UP LONG S BAL |
00643169103498 | BAYONET 2125-157 MURPHY UP SHRT S BAL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MURPHYSCOPE 75082983 2043471 Dead/Cancelled |
Clarus Medical Systems, Inc. 1996-04-03 |