Lighted Magnetic Foreign Body Removal Tool
- Primary DI
- 00714646001627
- Brand
- Lighted Magnetic Foreign Body Removal Tool
- Company
- Bionix, LLC
- Model
- 3521
- Catalog number
- 3521
- Device description
- Lighted Magnetic Foreign Body Remover - 1ct
- Published
- 2026-03-03
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KAK | PROBE, ENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KAK | Probe, Ent | Ear, Nose, Throat | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00714646001627 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00714646001627 | 00714646001627 | 714646001627 | 0714646001627 |
GMDN Terms#
| Term | Definition |
|---|---|
| Abdominal/ENT/orthopaedic surgical probe, single-use | A slender, rod-like, hand-held manual surgical instrument intended to be used to explore cavities, wounds or fistulas during abdominal, ENT, and/or orthopaedic surgical interventions; it does not include stereotactic devices and is not dedicated to endoscopy. It may have a blunt bulbous, paddle-like, or pointed tip, may be single- or double-ended, and the shaft may be straight, bent or hooked. It is made of rigid or flexible metallic and/or synthetic polymer material. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)551-7096 | Bionix@bionix.com |
Regulatory Flags#
- DUNS number
- 117844489
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Manufacturing date on label
- true
Other Devices From This Company#
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| 00859911004429 | Green MicroLoop® | 1222 | 1222 | 2021-12-10 |
| 00859911004436 | Orange ControLoop® | 2999 | 2999 | 2021-12-10 |
| 00859911004443 | Red AngleLoop® | 3444 | 3444 | 2021-12-10 |
| 00859911004450 | Purple VersaLoop® | 4111 | 4111 | 2021-12-10 |
| 00859911004467 | Blue InfantScoop® | 4888 | 4888 | 2021-12-10 |
| 00859911004474 | Yellow CeraSpoon® | 6333 | 6333 | 2021-12-10 |
| 00859911004481 | White FlexLoop® | 9555 | 9555 | 2021-12-10 |
| 00859911004528 | Lighted AngleLoop® | 2210 | 2210 | 2021-12-10 |
| 00859911004535 | Lighted MicroLoop® | 2220 | 2220 | 2021-12-10 |
| 00859911004542 | Lighted WaveCurette™ | 2230 | 2230 | 2021-12-10 |
| 00859911004559 | Lighted FlexLoop® | 2240 | 2240 | 2021-12-10 |
| 00859911004566 | Lighted Ear Curette™ Variety Pack | 2245 | 2245 | 2021-12-10 |
| 00859911004573 | Lighted CeraSpoon® | 2250 | 2250 | 2021-12-10 |
| 00859911004580 | Lighted InfantScoop® | 2260 | 2260 | 2021-12-10 |
| 00859911004597 | Lighted VersaLoop® | 2270 | 2270 | 2021-12-10 |
| 00859911004603 | Lighted CeraPik™ | 2280 | 2280 | 2021-12-10 |
| 00859911004702 | Lighted Forceps for Foreign Body Removal | 2750 | 2750 | 2021-12-10 |
| 00859911004726 | Lighted Placement Tool | 2850 | 2850 | 2022-08-08 |
| 00714646000675 | Ear Wax Removal Kit | 702 | 702 | 2024-07-11 |
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| 00724995270957 | V. Mueller | STERIS Deutschland GmbH | KAK | 2026-09-25 |
| 04054462915071 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-25 |
| 04054462915088 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-25 |
| 04054462915095 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-25 |
| 04054462915101 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-25 |
| 04054462905751 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-21 |
| 04054462901203 | evonos | evonos GmbH & Co. KG | KAK | 2026-08-18 |
| 00840183532963 | BR Surgical, LLC | BR Surgical, LLC | KAK | 2026-07-17 |
| 00840183532970 | BR Surgical, LLC | BR Surgical, LLC | KAK | 2026-07-17 |
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| 09348811005106 | INKA | The Trustee for KAISER FAMILY TRUST | KAK | 2026-03-18 |
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