FENTEX
- Primary DI
- 04250407772840
- Brand
- FENTEX
- Company
- FENTEX medical GmbH
- Model
- 443514FX
- Catalog number
- 443514FX
- Device description
- Salivary Duct Probe by Bowman cylindric, silver size 3/4
- Published
- 2022-12-12
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
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 |
|---|---|---|---|---|
| 04250407772840 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04250407772840 | 04250407772840 | 4250407772840 |
GMDN Terms#
| Term | Definition |
|---|---|
| Ophthalmic surgical probe, reusable | A slender, rod-like, hand-held manual surgical instrument intended to be used during an ophthalmic procedure to explore, measure, and/or manipulate ocular tissues (e.g., retraction/manipulation of intraocular structures, lens nucleus splitting, removal of foreign bodies in the eye, LASIK flap lifting); it is neither intended to cut tissue nor hook muscles. It is available with a variety of tip shapes including blunt bulbous, hook and T-shape, and the shaft may be straight or bent; it is made of flexible or rigid metallic and/or synthetic polymer material. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +4974679496212 | s.renner@fentexmedical.com |
Regulatory Flags#
- DUNS number
- 507221724
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04250407737245 | FENTEX | 443530FX | 443530FX | 2022-12-12 |
| 04250407772727 | FENTEX | 443516FX | 443516FX | 2022-12-12 |
| 04250407774301 | FENTEX | 443512FX | 443512FX | 2022-12-12 |
| 04250407774318 | FENTEX | 443511FX | 443511FX | 2022-12-12 |
| 04250407774325 | FENTEX | 443510FX | 443510FX | 2022-12-12 |
| 04250407774332 | FENTEX | 443509FX | 443509FX | 2022-12-12 |
| 04250407774349 | FENTEX | 443539FX | 443539FX | 2022-12-12 |
| 04250407775131 | FENTEX | 443531FX | 443531FX | 2022-12-12 |
| 04250407715588 | FENTEX | 154100FX | 154100FX | 2022-12-08 |
| 04250407715595 | FENTEX | 154200FX | 154200FX | 2022-12-08 |
| 04250407715601 | FENTEX | 154300FX | 154300FX | 2022-12-08 |
| 04250407715618 | FENTEX | 154400FX | 154400FX | 2022-12-08 |
| 04250407715625 | FENTEX | 154500FX | 154500FX | 2022-12-08 |
| 04250407715632 | FENTEX | 154600FX | 154600FX | 2022-12-08 |
| 04250407715649 | FENTEX | 154700FX | 154700FX | 2022-12-08 |
| 04250407715663 | FENTEX | 154800FX | 154800FX | 2022-12-08 |
| 04250407715670 | FENTEX | 155102FX | 155102FX | 2022-12-08 |
| 04250407715687 | FENTEX | 155104FX | 155104FX | 2022-12-08 |
| 04250407715694 | FENTEX | 155105FX | 155105FX | 2022-12-08 |
| 04250407715700 | FENTEX | 155106FX | 155106FX | 2022-12-08 |
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| 00714646001627 | Lighted Magnetic Foreign Body Removal Tool | Bionix, LLC | KAK | 2026-03-03 |
| 09348811115836 | INKA | The Trustee for KAISER FAMILY TRUST | KAK | 2025-11-25 |
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| 04250676740663 | Bowman salivary duct probe | Spiggle & Theis Medizintechnik GmbH | KAK | 2025-09-29 |
| 04250676740687 | Bowman salivary duct probe | Spiggle & Theis Medizintechnik GmbH | KAK | 2025-09-29 |
| 04250676740694 | Bowman salivary duct probe | Spiggle & Theis Medizintechnik GmbH | KAK | 2025-09-29 |
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