SCANLAN® Heifetz™ Temporary Clips and Appliers
- Primary DI
- 00846159004137
- Brand
- SCANLAN® Heifetz™ Temporary Clips and Appliers
- Company
- SCANLAN INTERNATIONAL INC
- Model
- 3795-01A
- Catalog number
- 3795-01A
- Device description
- SCANLAN® Heifetz™ Clip Applier, angled, 7-1/4"/18.5 cm
- Published
- 2019-11-26
- 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 |
|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00846159004137 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00846159004137 | 00846159004137 | 846159004137 | 0846159004137 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical soft-tissue manipulation forceps, tweezers-like, reusable | A hand-held, manual, open-surgery instrument designed to facilitate grasping and manipulation of soft-tissues. It has a tweezers-like design (may be a micro/fine instrument) 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 made of high-grade stainless steel, available in various sizes, and may have carbide inserts at the working end. It is not an electrosurgical device and not dedicated to ophthalmic surgery. This is a reusable device intended to be sterilized prior to use. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| 651-298-0997 | VanderpoelW@Scanlangroup.com |
Regulatory Flags
- DUNS number
- 023055619
- 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
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