NA
- Primary DI
- 34546540427909
- Brand
- NA
- Company
- STRYKER CORPORATION
- Model
- 5290635000
- Catalog number
- 5290-635-000
- Device description
- 3.5 mm ENT Precision Cutter Aggressive Serrated ESSx/HUMMER 4 8.0 cm Working Length
- Published
- 2016-09-23
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Ear, Nose, Throat | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 34546540427909 | Package | GS1 | 5 | In Commercial Distribution |
| 04546540427908 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 34546540427909 | 34546540427909 | |
| 04546540427908 | 04546540427908 | 4546540427908 |
GMDN Terms
| Term | Definition |
|---|---|
| Sagittal surgical saw blade, single-use | A sterile, flat surgical cutting instrument, usually made of high-grade stainless steel, with a serrated edge designed for attachment to a dedicated powered saw used for cutting bone/tissue during orthopaedic or oral surgery. This device is designed with the cutting teeth arranged in an arc at the distal end pointing directly forward. It cuts when the blade is powered in a rapid oscillating (side to side) movement. This type of blade allows a frontal cutting action to be applied within a restricted area. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 8 | Centimeter |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)253-3210 | Inst.Stryker.cs@Stryker.com |
Regulatory Flags
- DUNS number
- 196548481
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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