FDA UDI In Commercial Distribution 🇺🇸 United States

Acupac®

DI: B715412008P0 · Model: 4120-08P · FRICKE INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Acupac®
Primary DI
B715412008P0
Version / Model
4120-08P
Catalog Number
4120-08P
Company Name
FRICKE INTERNATIONAL, INC.
Labeler DUNS
957630726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-23
Public Version
2
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
e058665f-3dd1-4106-a2c3-420c3d2ee3d6

Device Description

Acupac® 30 Medium

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
EBI Resin, Denture, Relining, Repairing, Rebasing

GMDN Terms

Code Name
16730 Dental appliance fabrication material, resin

Identifiers

Type ID
Primary B715412008P0

Customer Contacts

Phone
630-540-1900

Device Sizes

Type Value Unit Text
Weight 5 Pound