FDA UDI In Commercial Distribution 🇺🇸 United States

Vonflex S Medium

DI: 08809254456456 · Model: VF305-SMN0 · VERICOM CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vonflex S Medium
Primary DI
08809254456456
Version / Model
VF305-SMN0
Company Name
VERICOM CO., LTD.
Labeler DUNS
689698269
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
3fb9e349-312f-4209-a45f-3b91844d0bbd

Device Description

Hydrophilic Vinyl Polysiloxane Impression Material ; Medium bodied Consistency ; Normal Set ; 50ml x 1 cartridge

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ELW Material, Impression

GMDN Terms

Code Name
35866 Silicone dental impression material

Identifiers

Type ID
Primary 08809254456456

Customer Contacts

Phone
+82314412881

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 24 Degrees Celsius