FDA UDI In Commercial Distribution 🇺🇸 United States

Plugger

DI: 00889989069617 · Model: 973-0221 · ORMCO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Plugger
Primary DI
00889989069617
Version / Model
973-0221
Company Name
ORMCO CORPORATION
Labeler DUNS
154614119
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-08
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2cada23b-8c73-49d3-94e9-0ddd9f9b44e6

Device Description

PLUGGER, THIN TIP (.5mm)

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
41876 Endodontic plugger

Identifiers

Type ID
Primary 00889989069617

Customer Contacts

Phone
+18005377123