Bioseal Inc.
- Primary DI
- 10630094198023
- Brand
- Bioseal Inc.
- Company
- BIOSEAL
- Model
- 19802/50
- Device description
- Alkaline Battery
- Published
- 2023-12-07
- 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 |
|---|---|
| MOQ | BATTERY, REPLACEMENT, RECHARGEABLE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MOQ | Battery, Replacement, Rechargeable | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10630094198023 | Package | GS1 | 50 | In Commercial Distribution |
| 00630094198026 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10630094198023 | 10630094198023 | ||
| 00630094198026 | 00630094198026 | 630094198026 | 0630094198026 |
GMDN Terms#
| Term | Definition |
|---|---|
| Disposable battery pack | A group of battery cells (e.g., lithium ion cells) held within a container that is sterile used to provide temporary electrical energy to operate a medical device, typically when it is not possible, intentional, or convenient to connect the device being powered to a mains electricity (AC-powered) electrical outlet. This device is typically designed to power cordless surgical power tools (e.g., a non-rechargeable battery-powered surgical drilling system handpiece) and is non-rechargeable. 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 |
|---|---|---|---|---|
| 00630094198514 | Bioseal Inc. | 19851NS/100 | 2023-12-07 | |
| 00630094171470 | Bioseal Inc. | 17147/01 | 2023-09-18 | |
| 00630094017501 | Bioseal Inc. | 1750/50 | 2023-09-25 | |
| 10630094481026 | Bioseal Inc. | DURA102/100 | 2025-05-29 | |
| 10630094481231 | Bioseal Inc. | DURA123/100 | 2025-05-29 | |
| 10630094483006 | Bioseal Inc. | DURA300/100 | 2025-05-29 | |
| 10630094485055 | Bioseal Inc. | DURA505/100 | 2025-05-29 | |
| 10630094485123 | Bioseal Inc. | DURA512/100 | 2025-05-29 | |
| 10630094487028 | Bioseal Inc. | DURA702/100 | 2025-05-29 | |
| 10630094487059 | Bioseal Inc. | DURA705/100 | 2025-05-29 | |
| 10630094487301 | Bioseal Inc. | DURA730/100 | 2025-05-29 | |
| 10630094489022 | Bioseal Inc. | DURA902/100 | 2025-05-29 | |
| 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 |
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