Tubifast®
GUDID 05055158000865
Tubifast Leggings 2 - 5 yrs x 6
Mölnlycke Health Care AB
Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable| Primary Device ID | 05055158000865 |
| NIH Device Record Key | cf2670a8-230a-4803-b6b5-ea444e5bc33f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tubifast® |
| Version Model Number | 992013 |
| Company DUNS | 631770658 |
| Company Name | Mölnlycke Health Care AB |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05055158000711 [Primary] |
| GS1 | 05055158000865 [Package] Contains: 05055158000711 Package: PACK_OR_INNER_PACK [6 Units] In Commercial Distribution |
| GS1 | 07332551959180 [Package] Package: CASE [5 Units] In Commercial Distribution |
FDA Product Code
| FQM | BANDAGE, ELASTIC |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-31 |
| Device Publish Date | 2022-10-21 |
On-Brand Devices [Tubifast®]
| 07332551896119 | T/Fast Gloves Small Child |
| 07332551870690 | T/Fast Gloves XS Child |
| 07332551870645 | T/Fast Gloves S/M Adult-M/L Child |
| 07332551870591 | T/Fast Gloves M/L Adult |
| 07332551935573 | Tubifast 2-Way Stretch Purple 10m |
| 05055158008779 | Tubifast 2-Way Stretch Yellow 10m |
| 05055158008731 | Tubifast 2-Way Stretch Blue 10m |
| 05055158008694 | Tubifast 2-Way Stretch Green 10m |
| 05055158008656 | Tubifast 2-Way Stretch Red 10m |
| 05055158000902 | Tubifast Socks One Size x 6 |
| 07332551959128 | Tubifast Vest 11 - 14 yrs x 6 |
| 05055158000834 | Tubifast Vest 8 - 11 yrs x 6 |
| 07332551959067 | Tubifast Vest 5 - 8 yrs x 6 |
| 05055158000810 | Tubifast Vest 2 - 5 yrs x 6 |
| 05055158000803 | Tubifast Vest 6-24Mths x6 |
| 07332551959272 | Tubifast Leggings 11 - 14 yrs x 6 |
| 07332551959241 | Tubifast Leggings 8 - 11 yrs x 6 |
| 07332551959210 | Tubifast Leggings 5 - 8 yrs x 6 |
| 05055158000865 | Tubifast Leggings 2 - 5 yrs x 6 |
| 07332551959159 | Tubifast Leggings 6 - 24mths x 6 |
| 07332551940270 | Tubifast 2-Way Stretch Yellow 5m 10x6pcs |
Trademark Results [Tubifast]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TUBIFAST 73382636 1350244 Live/Registered |
SETON PRODUCTS LIMITED 1982-08-30 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.