FDA UDI
In Commercial Distribution
🇺🇸 United States
Biatain Silicone Fit
DI: 05708932761598
·
Model: 37546
·
Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Biatain Silicone Fit
- Primary DI
- 05708932761598
- Version / Model
- 37546
- Catalog Number
- 37546
- Company Name
- Coloplast A/S
- Labeler DUNS
- 305524696
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-12-22
- Public Version
- 1
- Public Version Date
- 2024-01-01
- Public Version Status
- New
- Public Device Record Key
- 0b811ede-79d0-49dc-8ba3-5698eeae9208
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- Yes
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- Yes
- 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 |
|---|---|---|---|---|
| NAD | Dressing, wound, occlusive | General, Plastic Surgery | 878.4020 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 44970 | Exudate-absorbent dressing, non-gel, non-antimicrobial | A wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 05708932761604 | GS1 | Shipper Box | 12 | In Commercial Distribution | |
| Package | 05708932761611 | GS1 | Retail Box | 5 | In Commercial Distribution | |
| Primary | 05708932761598 | GS1 |
Customer Contacts
- Phone
- +1(800)533-0464
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Width | 6.6 | Inch | |
| Device Size Text, specify | Pad Length - cm 14.1 | ||
| Length | 7.2 | Inch | |
| Device Size Text, specify | Pad Length - in 5.6 | ||
| Device Size Text, specify | Pad Width - cm 13.4 | ||
| Width | 16.9 | Centimeter | |
| Length | 18.2 | Centimeter | |
| Device Size Text, specify | Dressing Shape Heel | ||
| Device Size Text, specify | Pad Width - in 5.3 |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Keep away from sunlight. Do not use if package is damaged and consult IFU.