Integra®
- Primary DI
- 10381780086758
- Brand
- Integra®
- Company
- INTEGRA LIFESCIENCES PRODUCTION CORPORATION
- Model
- 3740051
- Catalog number
- 3740051
- Device description
- Integra® Bishop-Harmon Tissue Forceps, 1*2 Teeth, 0.85 mm Teeth
- Published
- 2018-10-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GEN | FORCEPS, GENERAL & PLASTIC SURGERY |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GEN | Forceps, General & Plastic Surgery | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10381780086758 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780086758 | 10381780086758 |
GMDN Terms#
| Term | Definition |
|---|---|
| Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable | A hand-held manual surgical instrument designed to facilitate the 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, 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 reusable device intended to be sterilized prior to use. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)654-2873 | custsvcnj@integralife.com |
Regulatory Flags#
- DUNS number
- 081277700
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10381780024507 | Integra® Jarit® | 100539 | 100-539 | 2018-01-22 |
| 10381780024514 | Integra® Jarit® | 100540 | 100-540 | 2018-01-22 |
| 10381780031901 | Integra® Miltex® | 27-202 | 27-202 | 2015-09-22 |
| 10381780031918 | Integra® Miltex® | 27-204 | 27-204 | 2015-09-22 |
| 10381780031925 | Integra® Miltex® | 27-206 | 27-206 | 2015-09-22 |
| 10381780031932 | Integra® Miltex® | 27-208 | 27-208 | 2015-09-22 |
| 10381780031949 | Integra® Miltex® | 27-210 | 27-210 | 2015-09-22 |
| 10381780031956 | Integra® Miltex® | 27-212 | 27-212 | 2015-09-22 |
| 10381780063865 | Integra® Miltex® | 4-515C | 4-515C | 2018-02-15 |
| 10381780063872 | Integra® Miltex® | 4-522 | 4-522 | 2018-02-15 |
| 10381780063896 | Integra® Miltex® | 4611 | 4611 | 2018-02-15 |
| 10381780063902 | Integra® Miltex® | 4615 | 4615 | 2018-02-15 |
| 10381780064206 | Integra® Miltex® | 33-38 | 33-38 | 2018-02-14 |
| 10381780128779 | Integra® Miltex® | 30-1740 | 30-1740 | 2016-08-03 |
| 10381780133810 | Integra® Jarit® | 320437 | 320-437 | 2016-08-12 |
| 10381780134503 | Integra® Jarit® | 653101 | 653101 | 2018-01-15 |
| 10381780136408 | Integra® Jarit® | X37254 | X37254 | 2016-08-14 |
| 10381780142874 | Integra® Jarit® | 230250 | 230-250 | 2016-08-14 |
| 10381780143048 | Integra® Jarit® | 320195 | 320-195 | 2016-08-14 |
| 10381780143055 | Integra® Jarit® | 320196 | 320-196 | 2016-08-14 |
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