Bioseal Inc.
- Primary DI
- 10630094043170
- Brand
- Bioseal Inc.
- Company
- BIOSEAL
- Model
- 4317/24
- Device description
- Penrose Drain
- Published
- 2024-01-18
- 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
Related Records
Product Codes
| Code | Name |
|---|---|
| GBX | CATHETER, IRRIGATION |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GBX | Catheter, Irrigation | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10630094043170 | Package | GS1 | 24 | In Commercial Distribution |
| 00630094043173 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10630094043170 | 10630094043170 | ||
| 00630094043173 | 00630094043173 | 630094043173 | 0630094043173 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical capillary wound drain, luminal, synthetic polymer | A sterile device with a lumen(s) designed to establish a passive egress for the removal of fluid (drainage of blood, lymph, exudate) from a surgical wound to minimize its accumulation and risk of wound infection; it is not dedicated to a particular anatomical wound. It is typically inserted into the wound by a surgeon in the operating room (OR) after the completion of an inpatient or outpatient procedure. It is typically made of radiopaque silicone and is available in various forms (e.g., Penrose type, tubular with side holes, multi-tubular). This is a single-use device. |
Sterilization Methods
| Method |
|---|
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
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00630094481029 | Bioseal Inc. | DURA102/100 | 2025-05-29 | |
| 00630094481234 | Bioseal Inc. | DURA123/100 | 2025-05-29 | |
| 00630094483009 | Bioseal Inc. | DURA300/100 | 2025-05-29 | |
| 00630094485058 | Bioseal Inc. | DURA505/100 | 2025-05-29 | |
| 00630094485126 | Bioseal Inc. | DURA512/100 | 2025-05-29 | |
| 00630094487021 | Bioseal Inc. | DURA702/100 | 2025-05-29 | |
| 00630094487052 | Bioseal Inc. | DURA705/100 | 2025-05-29 | |
| 00630094487304 | Bioseal Inc. | DURA730/100 | 2025-05-29 | |
| 00630094489025 | Bioseal Inc. | DURA902/100 | 2025-05-29 | |
| 00630094480503 | Bioseal Inc. | DURA050/100 | 2025-05-28 | |
| 10630094292240 | Bioseal Inc. | 32-922-4/20 | 2024-01-10 | |
| 10630094335404 | Bioseal Inc. | 33-540/20 | 2024-01-10 | |
| 10630094055111 | Bioseal Inc. | 551S/20 | 2024-01-29 | |
| 10630094055135 | Bioseal Inc. | 551L/20 | 2024-01-29 | |
| 10630094055142 | Bioseal Inc. | 551M/20 | 2024-01-29 | |
| 10630094055197 | Bioseal Inc. | 551R/20 | 2024-01-29 | |
| 10630094061501 | Bioseal Inc. | 6150/25 | 2024-01-29 | |
| 10630094061518 | Bioseal Inc. | 6151/25 | 2024-01-29 | |
| 10630094061525 | Bioseal Inc. | 6152/50 | 2024-01-29 | |
| 10630094064243 | Bioseal Inc. | 6424/120 | 2024-01-29 |
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