FDA UDI In Commercial Distribution 🇺🇸 United States

OpaFit

DI: D815OPAFIT3HCLG0 · Model: OPAFIT3HCLG · OPA DENTAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OpaFit
Primary DI
D815OPAFIT3HCLG0
Version / Model
OPAFIT3HCLG
Catalog Number
OPAFIT3HCLG
Company Name
OPA DENTAL LLC
Labeler DUNS
053308044
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-16
Public Version
1
Public Version Date
2021-08-24
Public Version Status
New
Public Device Record Key
3a04c3fe-0f74-4e61-8a6d-b43bcc51105d

Device Description

VPS Heavy Body impression material 380ml Cartridge

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
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 D815OPAFIT3HCLG0