FDA UDI Not in Commercial Distribution 🇺🇸 United States

SALVIN RENOVIX

DI: 03760193181982 · Model: MCG 12 23 U · DILON TECHNOLOGIES FRANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SALVIN RENOVIX
Primary DI
03760193181982
Version / Model
MCG 12 23 U
Catalog Number
RENOVIX-20x30
Company Name
DILON TECHNOLOGIES FRANCE
Labeler DUNS
279346203
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-25
Public Version
4
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
8bb47987-7d60-4348-8758-450d18b95278
Distribution End Date
2019-05-21

Device Description

Collagen Guided Healing Membrane

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NPL Barrier, Animal Source, Intraoral

GMDN Terms

Code Name
58709 Collagen dental regeneration membrane

Identifiers

Type ID
Primary 03760193181982

Customer Contacts

Phone
+33486573610

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Width 20 Millimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
2 – 30 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Dry place away from humidity