| Primary Device ID | 17310231150000 |
| NIH Device Record Key | 58066fdf-8700-4f1d-a2dd-de5bcc791acd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PractiPal |
| Version Model Number | MultiDappen |
| Catalog Number | 115000 |
| Company DUNS | 353954381 |
| Company Name | Directa AB |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 17310231150000 [Primary] |
| FSM | Tray, Surgical, Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-15 |
| Device Publish Date | 2022-12-07 |
| 17310231151205 | Clips |
| 17310231150048 | Foam Large |
| 17310231150031 | Foam |
| 17310231150024 | Waste Cup |
| 17310231150017 | MultiPoint |
| 17310231150000 | MultiDappen |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PRACTIPAL 79017852 3225274 Live/Registered |
Directa AB 2005-08-17 |
![]() PRACTIPAL 76215465 2757970 Dead/Cancelled |
ADELS, VERENA 2001-02-23 |
![]() PRACTIPAL 76215465 2757970 Dead/Cancelled |
LIMMER, HELMUT 2001-02-23 |