Iris Retractor
- Primary DI
- 00192896102798
- Brand
- Iris Retractor
- Company
- SONTEC INSTRUMENTS, INC.
- Model
- 12-4800
- Device description
- Rizzuti Iris Retractor and Lens Expressor
- Published
- 2020-06-30
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HNI | Retractor, ophthalmic |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HNI | Retractor, Ophthalmic | Ophthalmic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00192896102798 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00192896102798 | 00192896102798 | 192896102798 | 0192896102798 |
GMDN Terms
| Term | Definition |
|---|---|
| Ocular hook/spatula/manipulator, reusable | A hand-held, blunt, manual ophthalmic surgical instrument intended for manipulation/retraction of intraocular structures, lens nucleus splitting/manipulation, removal of foreign bodies in the eye, corneal manipulation (e.g., LASIK flap lifting), and/or in situ intraocular lens (IOL) manipulation; it is neither intended to cut tissue nor hook muscles. It may be of single- or double-ended design with a working end(s) designed as a hook, spatula, or other manipulator (often Y-shaped); it is not a curette, loop, trabeculotome, spoon, or inner limiting membrane (ILM) scraper. This is a reusable device intended to be sterilized prior to use. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Dry Heat Sterilization;Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)821-7496 | info@sontecinstruments.com |
Regulatory Flags
- DUNS number
- 040729840
- 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
- true
- Sterilization required before use
- true
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