HEELIFT AFO® Ultra
- Primary DI
- G0648317270053020
- Brand
- HEELIFT AFO® Ultra
- Company
- POSITION HEALTH, LLC
- Model
- 831727005302
- Catalog number
- 831727005302
- Device description
- HEELIFT AFO® Ultra Suspension Boot, Heel Protector, Impact Protector, Smooth Foam, Fluid-repellent Fabric lining, Semi-rigid splint, Non-slip Traction Sole. Size Standard. Includes accessory HEELIFT® ARW (G0648317270098980)
- Published
- 2022-12-09
- 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 |
|---|
| FMP | Protector, Skin Pressure |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FMP | Protector, Skin Pressure | General Hospital | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| G0648317270053020 | Primary | HIBCC | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Ankle/foot orthosis | A prefabricated (non-customized) externally applied and wearable 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 patient adaptable plantar inserts. This is a reusable device. |
Regulatory Flags
- DUNS number
- 116685742
- 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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