| Primary Device ID | 10381780045144 |
| NIH Device Record Key | 8922097e-5f5f-405a-bf84-62c8715f4ab7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FOREFOOT |
| Version Model Number | 119006ND |
| Catalog Number | 119006 |
| Company DUNS | 536935331 |
| Company Name | NEWDEAL |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Outer Diameter | 2.2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 41 Millimeter |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10381780045144 [Primary] |
| HTW | BIT, DRILL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
[10381780045144]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-01-07 |
| Device Publish Date | 2020-12-30 |
| 10381780064398 | The principal of the FOREFOOT sets is to propose a group of implants (screws and staples) and th |
| 10381780045151 | Sterile drill for the introduction of the compression staples or screws. |
| 10381780045144 | Non-sterile drill for the introduction of compression staples or screws. |