Capsulorhexis Forceps, Utrata Tips, 12mm Curved Shafts, Round Handles
- Primary DI
- 05060411983007
- Brand
- Capsulorhexis Forceps, Utrata Tips, 12mm Curved Shafts, Round Handles
- Company
- DTR MEDICAL LIMITED
- Model
- CXF2001
- Published
- 2026-06-10
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| HNR | Forceps, Ophthalmic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HNR | Forceps, Ophthalmic | Ophthalmic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05060411983014 | Package | GS1 | 20 | In Commercial Distribution |
| 05060411983007 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05060411983014 | 05060411983014 | 5060411983014 |
| 05060411983007 | 05060411983007 | 5060411983007 |
GMDN Terms#
| Term | Definition |
|---|---|
| Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use | A sterile, hand-held manual surgical instrument designed to facilitate grasping, manipulation or clamping of, and/or removal of foreign bodies from, ophthalmic soft-tissues (ocular tissues, eyelids), and may be pointed for capsulorhexis. It has a conventional (self-opening) or reverse-action (self-closing) tweezers-like design, with variously designed tips at the working end, whereby the blades are designed to be opened/closed by squeezing between the fingers (i.e., without ring handles); it is not probe-like in design (i.e., not cannulated). It is typically made of metal, available in various sizes, and may have carbide inserts at the working end. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep Dry / Keep out of Sunlight |
Regulatory Flags#
- DUNS number
- 424066509
- 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
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 00860015282033 | Intrace USA | PILOTIS TECH LLC | HNR | 2026-07-03 |
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