SUGITA ANEURYSM CLIP
- Primary DI
- 04946329060799
- Brand
- SUGITA ANEURYSM CLIP
- Company
- MIZUHO CORPORATION
- Model
- 07-940-13
- Catalog number
- 07-940-13
- Device description
- TYPE: LARGE, PERMANENT, No.13 RANGE: 120-165gf(1.18-1.62N) MATERIAL: ISO 5832-7/ASTM F1058G2 BLADE: BAYONET MAXIMUM OPENING: 11.0mm GRIP SURFACE: SERRATED
- Published
- 2015-10-10
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HCI | Applier, Aneurysm Clip |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HCI | Applier, Aneurysm Clip | Neurology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04946329060799 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04946329060799 | 04946329060799 | 4946329060799 |
GMDN Terms
| Term | Definition |
|---|---|
| Aneurysm clip, sterile | A sterile, metallic device intended to be permanently implanted around the neck of an aneurysm (a balloon-like sac formed on a blood vessel) for occlusion, to prevent it from bleeding or bursting and to isolate it from the rest of the vessel. The device is typically an alpha-shaped coil spring, with blades that open like jaws, that comes with a dedicated applier for application to the aneurysm. The device is available in a variety of sizes and its blades may be straight or curved. It is typically used to treat intracranial aneurysms; it may also be used to prevent bleeding from small blood vessels. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 10 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| 9999999999 | regulatory@mizuho.co.jp |
Regulatory Flags
- DUNS number
- 690677802
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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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