FDA UDI
In Commercial Distribution
🇺🇸 United States
Eigr™ Waveguide
DI: 00816728020059
·
Model: Narrow / Flat, LC
·
INVUITY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Eigr™ Waveguide
- Primary DI
- 00816728020059
- Version / Model
- Narrow / Flat, LC
- Catalog Number
- CEW1NF
- Company Name
- INVUITY, INC.
- Labeler DUNS
- 175697908
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-22
- Public Version
- 4
- Public Version Date
- 2020-04-24
- Public Version Status
- Update
- Public Device Record Key
- cf9457e9-fe2f-4359-82ba-ce5f753a787b
Device Description
The Eigr Waveguide, Narrow/Flat, LC is intended to provide surgical site illumination from a high intensity light source.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- Yes
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| FST | Light, Surgical, Fiberoptic | General, Plastic Surgery | 878.4580 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 48036 | Surgical instrument fibreoptic light | A sterile device with a fibreoptic bundle core designed to be affixed to the surface of a surgical instrument, typically a retractor, to conduct cold light from a connected fibreoptic light cable and light source into a surgical wound for illumination during a surgical intervention. It typcially emits cold light only through its tip to eliminate glare, and may have a self-adhesive coating for attachment to the surgical instrument. This is a single-use device. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00816728020059 | GS1 |
Customer Contacts
- Phone
- 8667117768
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K090070 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | Angle: Flat | ||
| Device Size Text, specify | Width: Narrow |