MurphyScope
GUDID 00643169103498
BAYONET 2125-157 MURPHY UP SHRT S BAL
MEDTRONIC PS MEDICAL, INC.
Flexible fibreoptic neuroscope Flexible fibreoptic neuroscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope Flexible fibreoptic intracranial/spinal endoscope| Primary Device ID | 00643169103498 |
| NIH Device Record Key | d508a4a7-a4dd-4f3b-8c4d-7f27d234a35b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MurphyScope |
| Version Model Number | 2125-157 |
| 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 |
Customer Support Contacts
Device Dimensions
| 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 |
Operating and Storage Conditions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169103498 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K010341
FDA Product Code
| GWG | ENDOSCOPE, NEUROLOGICAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-06-13 |
On-Brand Devices [MurphyScope]
| 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 |
Trademark Results [MurphyScope]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MURPHYSCOPE 75082983 2043471 Dead/Cancelled |
Clarus Medical Systems, Inc. 1996-04-03 |
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