FDA UDI In Commercial Distribution 🇺🇸 United States

HU-FRIEDY

DI: 10889950105815 · Model: PLGROMP1X · HU-FRIEDY MFG. CO., LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HU-FRIEDY
Primary DI
10889950105815
Version / Model
PLGROMP1X
Catalog Number
PLGROMP1X
Company Name
HU-FRIEDY MFG. CO., LLC
Labeler DUNS
005085972
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-12
Public Version
1
Public Version Date
2020-11-20
Public Version Status
New
Public Device Record Key
b2abcd8d-7933-41cf-b559-30dd09c5ca85

Device Description

Rompen Plugger, Buccal/Lingual

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
EKG CONDENSER, AMALGAM AND FOIL, OPERATIVE

GMDN Terms

Code Name
41876 Endodontic plugger

Identifiers

Type ID
Primary 10889950105815

Customer Contacts