MEMFIX
- Primary DI
- 07630031718242
- Brand
- MEMFIX
- Company
- Institut Straumann AG
- Model
- Fixation Screws
- Catalog number
- 042.702V5
- Device description
- Crosshead mini-screws D1.5mm, L12mm
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DZL | SCREW, FIXATION, INTRAOSSEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DZL | Screw, Fixation, Intraosseous | Dental | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K955369 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07630031718242 | Primary | GS1 | 0 | |
| 07630031747136 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07630031718242 | 07630031718242 | 7630031718242 |
| 07630031747136 | 07630031747136 | 7630031747136 |
GMDN Terms#
| Term | Definition |
|---|---|
| Screw endosteal dental implant, one-piece | A sterile device made of alloplastic materials [e.g., titanium (Ti), stainless steel, ceramic] intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture). It is a one-piece device composed of an anchorage portion (implant body) in the form of a threaded screw that is implanted into bone, and a retention portion (implant abutment) that protrudes through gingival tissues to support the prosthesis. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 12 | Millimeter |
| Outer Diameter | 1.5 | Millimeter |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)448-8168 | info.usa@straumann.com |
Regulatory Flags#
- DUNS number
- 483599259
- Device count
- 5
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 07630031778086 | NA | surgically Invasive Instruments | 066.5063 | 2026-06-03 |
| 07630031778093 | NA | surgically Invasive Instruments | 066.5064 | 2026-06-03 |
| 07630031778109 | NA | surgically Invasive Instruments | 066.5065 | 2026-06-03 |
| 07630031778116 | NA | surgically Invasive Instruments | 066.5066 | 2026-06-03 |
| 07630031778123 | NA | surgically Invasive Instruments | 066.5067 | 2026-06-03 |
| 07630031778130 | NA | surgically Invasive Instruments | 066.5068 | 2026-06-03 |
| 07630031778147 | NA | surgically Invasive Instruments | 066.5069 | 2026-06-03 |
| 07630031778154 | NA | surgically Invasive Instruments | 066.5070 | 2026-06-03 |
| 07630031778161 | NA | surgically Invasive Instruments | 066.5071 | 2026-06-03 |
| 07630031778192 | NA | surgically Invasive Instruments | 066.5074 | 2026-06-03 |
| 07630031778208 | NA | surgically Invasive Instruments | 066.5075 | 2026-06-03 |
| 07630031778215 | NA | surgically Invasive Instruments | 066.5076 | 2026-06-03 |
| 07630031778222 | NA | surgically Invasive Instruments | 066.5077 | 2026-06-03 |
| 07630031778239 | NA | surgically Invasive Instruments | 066.5078 | 2026-06-03 |
| 07630031778260 | NA | surgically Invasive Instruments | 066.5081 | 2026-06-03 |
| 07630031778277 | NA | surgically Invasive Instruments | 066.5082 | 2026-06-03 |
| 07630031778284 | NA | surgically Invasive Instruments | 066.5083 | 2026-06-03 |
| 07630031778291 | NA | surgically Invasive Instruments | 066.5084 | 2026-06-03 |
| 07630031778307 | NA | surgically Invasive Instruments | 066.5085 | 2026-06-03 |
| 07630031778338 | NA | surgically Invasive Instruments | 066.5088 | 2026-06-03 |
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