FDA UDI In Commercial Distribution 🇺🇸 United States

GPRO

DI: 00990010302204 · Model: GP2002 · Beyes Dental Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GPRO
Primary DI
00990010302204
Version / Model
GP2002
Catalog Number
GPRO F1
Company Name
Beyes Dental Canada Inc
Labeler DUNS
244261462
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-11
Public Version
1
Public Version Date
2023-05-19
Public Version Status
New
Public Device Record Key
705692a8-ec93-479c-8fbd-e5a231403417

Device Description

GPRO F1,Gutta-percha Obturation Filling Machine Tips included: 1x 23G 24mm, 1x 23G 28mm, 2x 25G 24mm

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
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKR Plugger, Root Canal, Endodontic

GMDN Terms

Code Name
45250 Endodontic obturation system handpiece, material extrusion

Identifiers

Type ID
Primary 00990010302204