PinnPoint™ Lok-Bar™ MTIL5053
GUDID 00841439105160
Transverse (45.5-47.5cm)
MEDTEC, INC.
Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system| Primary Device ID | 00841439105160 |
| NIH Device Record Key | 1bb09b1a-2c90-4bbc-8e9f-e41207d502b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PinnPoint™ Lok-Bar™ |
| Version Model Number | MTIL5053 |
| Catalog Number | MTIL5053 |
| Company DUNS | 103977526 |
| Company Name | MEDTEC, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841439105160 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K973842
FDA Product Code
| IXQ | Table, radiographic, stationary top |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-31 |
| Device Publish Date | 2017-08-02 |
On-Brand Devices [PinnPoint™ Lok-Bar™]
| 00841439105160 | Transverse (45.5-47.5cm) |
| 00841439105153 | Transverse (50-52cm) |
Trademark Results [PinnPoint]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PINNPOINT 87880191 not registered Dead/Abandoned |
Insight Investments LLC 2018-04-17 |
 PINNPOINT 77255066 not registered Dead/Abandoned |
PROLOGUE LABEL, INC. 2007-08-14 |
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