FDA UDI In Commercial Distribution 🇺🇸 United States

Duracetal

DI: 00842326102798 · Model: ACE-A30-270-B08 · The Myerson Company Limited
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Duracetal
Primary DI
00842326102798
Version / Model
ACE-A30-270-B08
Company Name
The Myerson Company Limited
Labeler DUNS
857278431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
096adaf9-0b8d-4a3a-8f29-0b0393fd5b30

Device Description

Shade A3 225g Bottle Thermoplastic Dental Resin

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
No
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
EHP Clasp, Preformed

GMDN Terms

Code Name
58288 Dental appliance fabrication material, thermoplastic

Identifiers

Type ID
Primary 00842326102798

Customer Contacts

Phone
18004232683

Device Sizes

Type Value Unit Text
Weight 225 Gram