FDA UDI
In Commercial Distribution
🇺🇸 United States
Refobacin® Bone Cement R
DI: 00880304990197
·
Model: 110034355
·
BIOMET
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Refobacin® Bone Cement R
- Primary DI
- 00880304990197
- Version / Model
- 110034355
- Catalog Number
- 110034355
- Company Name
- BIOMET
- Labeler DUNS
- 260930126
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-03-30
- Public Version
- 4
- Public Version Date
- 2021-07-14
- Public Version Status
- Update
- Public Device Record Key
- 5bae58a2-e615-415a-a635-79df6d5a5330
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- Yes
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Safe
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| MBB | BONE CEMENT, ANTIBIOTIC | Orthopedic | 888.3027 | 2 |
| LOD | BONE CEMENT | Orthopedic | 888.3027 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46059 | Orthopaedic cement, antimicrobial | A substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic prosthetic implants to the living bone and/or to fill voids in the case of bone pathologies, and to treat infected joint prostheses or osteomyelitis; it may also be used prophylactically in primary or uninfected revision total joint arthroplasty. It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene, and contains an antimicrobial agent. After application, this device cannot be reused. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00880304990197 | GS1 |
Customer Contacts
- Phone
- +0330475759100
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K171540 | 000 |