FDA UDI
In Commercial Distribution
🇺🇸 United States
Integra® MicroFrance®
DI: 10381780095460
·
Model: CEV81
·
INTEGRA MICROFRANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Integra® MicroFrance®
- Primary DI
- 10381780095460
- Version / Model
- CEV81
- Catalog Number
- CEV81
- Company Name
- INTEGRA MICROFRANCE
- Labeler DUNS
- 276593071
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-22
- Public Version
- 5
- Public Version Date
- 2023-04-26
- Public Version Status
- Update
- Public Device Record Key
- c3f87222-d1de-4e02-aac4-870d35a8f713
Device Description
Integra® MicroFrance® Sleeve for telescope 0°, 10 mm diameter
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- 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
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Moist Heat or Steam Sterilization
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | General, Plastic Surgery | 878.4400 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 44963 | Endoscope lens cleaner, gas/fluid, reusable | A device intended to be used for the in situ removal of blood/debris from the lens of an endoscope, or other endoscopic device, by directing gas or liquid to the edge of the lens. It is a tubular device, made from metal or plastic, intended to be attached to the inserted portion of the endoscopic device whereby gases/fluids are directed from a source (e.g., manual pump, drop infusion pack) to the lens. This is a reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 10381780095460 | GS1 |
Customer Contacts
- Phone
- +1(800)654-2873
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K080257 | 000 |