FDA UDI In Commercial Distribution 🇺🇸 United States

BIOPLAST®

DI: J01832702 · Model: 3270.2 · Scheu-Dental GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
BIOPLAST®
Primary DI
J01832702
Version / Model
3270.2
Company Name
Scheu-Dental GmbH
Labeler DUNS
317683787
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2024-11-17
Public Version
1
Public Version Date
2024-11-25
Public Version Status
New
Public Device Record Key
dc0c9f5e-b17e-4d47-80c4-47f88778a2fd

Device Description

BIOPLAST® 1.0 x 125 mm

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
Yes
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
KMY Positioner, Tooth, Preformed

GMDN Terms

Code Name
58288 Dental appliance fabrication material, thermoplastic

Identifiers

Type ID
Primary J01832702
Unit of Use J01832700

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius