MD Orthopaedics
- Primary DI
- 00810060886830
- Brand
- MD Orthopaedics
- Company
- MD ORTHOPAEDICS, INC.
- Model
- AFO-8-PRW
- Device description
- Ankle foot orthosis, prefabricated (pair), to be attached to abduction brace, L1930 x 2 AFO SIZE 8 PAIR GRAY
- Published
- 2020-10-05
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- true
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| KNP | Orthosis, Corrective Shoe |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| KNP | Orthosis, Corrective Shoe | Physical Medicine | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00810060886830 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Ankle/foot orthosis | An externally-applied appliance or apparatus intended to encompass the ankle joint, or the ankle and foot, to support, align, prevent, or correct orthopaedic deformities/injuries or to improve function of the ankle and/or foot through actions such as alignment, hinge-support, or dorsiflexion assistance. It may also be intended to offload and redistribute foot pressures that affect pedal circulation to improve blood flow and help heal diabetic foot ulcers or postsurgical wounds, and may include customizable plantar inserts. This is a single-patient device that can be reapplied to the patient during the treatment period (reusable) before being discarded. |
Regulatory Flags
- DUNS number
- 146220269
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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