NA
- Primary DI
- 20845854024833
- Brand
- NA
- Company
- Conmed Corporation
- Model
- 8054-8
- Catalog number
- 8054-8
- Device description
- LIGHT GUIDE 4.0MM
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FST | LIGHT, SURGICAL, FIBEROPTIC |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FST | Light, Surgical, Fiberoptic | General, Plastic Surgery | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K901035 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30845854024830 | Direct Marking | GS1 | 0 | |
| 20845854024833 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 30845854024830 | 30845854024830 |
| 20845854024833 | 20845854024833 |
GMDN Terms#
| Term | Definition |
|---|---|
| Fibreoptic light cable, reusable | A flexible fibreoptic cable that is designed to transport cold light from a light source to an instrument or other equipment, e.g., an endoscope or a headlight. The fibreoptic bundle is protected within a sheath and can be made of either glass or plastic fibres. Each end of the cable is encased in a metal connector that fits into the respective instruments/equipment and also protects the end of the fibreoptic bundle. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
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