Channel
GUDID 00613994840240
CHANNELSCOPE 2233-005 30K 13 CM
MEDTRONIC PS MEDICAL, INC.
Rigid optical neuroscope, single-use| Primary Device ID | 00613994840240 |
| NIH Device Record Key | c2c9feaf-a8fe-4cc5-a61d-bc842f7d4988 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Channel |
| Version Model Number | 2233-005 |
| 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
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 | 00613994840240 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K002572
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 | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2016-06-13 |
On-Brand Devices [Channel]
| 00613994840240 | CHANNELSCOPE 2233-005 30K 13 CM |
| 00643169103597 | NEUROENDOSCP 2232-004 CHANNEL 3.5 L 13 |
| 00643169103580 | NEUROENDOSCP 2232-003 CHANNEL 4.5 L 13 |
| 00643169103573 | NEUROENDOSCOPE 2232-002 CHANNEL 3.5 |
| 00643169103566 | NEUROENDOSCOPE 2232-001 CHANNEL 4.5 |
| 00613994965622 | CHANNELSCOPE 2233-002 30K 21.6 LNG |
Trademark Results [Channel]
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