AfterSwim® Water Removal
- Primary DI
- 00859911004016
- Brand
- AfterSwim® Water Removal
- Company
- Bionix, LLC
- Model
- 530-SD
- Catalog number
- 530-SD
- Device description
- AfterSwim Water Removal
- Published
- 2022-01-06
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- OTC
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KXF | APPLICATOR, ABSORBENT TIPPED, NON-STERILE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KXF | Applicator, Absorbent Tipped, Non-Sterile | General Hospital | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00859911004016 | Primary | GS1 | 0 | |
| 10859911004013 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00859911004016 | 00859911004016 | 859911004016 | 0859911004016 |
| 10859911004013 | 10859911004013 |
GMDN Terms#
| Term | Definition |
|---|---|
| Ear canal drying sponge | A hand-held absorbent wedge intended to be partially inserted into the external auditory canal of the ear to dry the canal by absorbing water accumulated from bathing, showering, swimming, or diving, typically to prevent canal inflammation associated with water exposure (otitis externa or Swimmer’s ear). It is made of a soft spongy material and typically has a flared design to prevent over insertion and eardrum damage. This is a single-use device. |
Contacts#
| Phone | |
|---|---|
| +1(800)551-7096 | Bionix@bionix.com |
Regulatory Flags#
- DUNS number
- 117844489
- Device count
- 12
- DM exempt
- true
- Premarket exempt
- true
- Lot or batch
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00859911004498 | Safe Ear Curette™ Variety Kit | 5777 | 5777 | 2021-12-10 |
| 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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