FDA UDI
Not in Commercial Distribution
🇺🇸 United States
Bioplate®
DI: M384813595US0
·
Model: 81-3595[US]
·
Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Bioplate®
- Primary DI
- M384813595US0
- Version / Model
- 81-3595[US]
- Catalog Number
- 81-3595[US]
- Company Name
- Bioplate, Inc.
- Labeler DUNS
- 838734093
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-06-10
- Public Version
- 7
- Public Version Date
- 2023-09-12
- Public Version Status
- Update
- Public Device Record Key
- e4b9c94c-64e6-48db-ba4f-7d9273530dcd
- Distribution End Date
- 2022-02-01
Device Description
5-Tab Zip Implant - 16 mm
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Moist Heat or Steam Sterilization
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| GXN | Plate, Cranioplasty, Preformed, Non-Alterable | Neurology | 882.5330 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46268 | Cranioplasty plate, non-alterable | An implantable shield designed to repair larger skull defects that is preformed before surgery and typically made of sheets of material [e.g., stainless steel, vitallium, titanium (Ti), plastic resins] that cannot be reshaped at the time of surgery without changing the physical or chemical properties of the material. The device is generally preformed with a central convex curvature matching the curvature of the forehead, side, or rear areas of the human adult skull; it is usually fixed to the intact cranial bones using screws and/or other fasteners. The device is used to repair defects due to injury, surgical intervention for tumour removal, congenital anomaly, or disease. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | M384813595US0 | HIBCC |
Customer Contacts
- Phone
- 888-246-7528
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K070901 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 16 | Millimeter |