Combifix™ Baseplate 151014
GUDID 00841439100820
Combifix™ Baseplate
MEDTEC, INC.
Radiological arm/leg positioner| Primary Device ID | 00841439100820 |
| NIH Device Record Key | ab4a0c45-48ec-41e1-8fa4-45538424f286 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Combifix™ Baseplate |
| Version Model Number | 151014 |
| Catalog Number | 151014 |
| 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 | 00841439100820 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K060737
FDA Product Code
| IYE | Accelerator, linear, medical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-05-31 |
| Device Publish Date | 2017-08-02 |
On-Brand Devices [Combifix™ Baseplate]
| 00841439111871 | Combifix™ Baseplate |
| 00841439100820 | Combifix™ Baseplate |
Trademark Results [Combifix]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COMBIFIX 74269878 not registered Dead/Abandoned |
E. R. Squibb & Sons, Inc. 1992-04-27 |
 COMBIFIX 72282148 0868948 Dead/Expired |
TESA S.A. 1967-10-09 |
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