Bioseal Inc.
- Primary DI
- 10630094174249
- Brand
- Bioseal Inc.
- Company
- BIOSEAL
- Model
- 17424/50
- Device description
- Foam Padding
- Published
- 2023-09-20
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- true
- Single use
- true
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 |
|---|
| 10630094174249 | Package | GS1 | 50 | In Commercial Distribution |
| 00630094174242 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 10630094174249 | 10630094174249 | | |
| 00630094174242 | 00630094174242 | 630094174242 | 0630094174242 |
GMDN Terms
| Term | Definition |
|---|
| General-purpose medical foam padding, single-use | A roll, sheet or preformed shape of synthetic latex foam material [e.g., styrene-butadiene rubber (SBR)] intended to be applied to and/or compress a local area of the body for various preventative/therapeutic applications (e.g., in compression bandaging, padding under casts and splints, padding for anatomical depressions), typically over intact and healthy skin. It is intended for use in the home or a clinical setting. This is a single-use device. |
Regulatory Flags
- DUNS number
- 186968939
- Device count
- 1
- DM exempt
- true
- 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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