FDA UDI In Commercial Distribution 🇺🇸 United States

HyFlex™ EDM

DI: E165600222811 · Model: 60022281 · Coltène/Whaledent GmbH + Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
HyFlex™ EDM
Primary DI
E165600222811
Version / Model
60022281
Catalog Number
60022281
Company Name
Coltène/Whaledent GmbH + Co. KG
Labeler DUNS
315494443
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2022-09-22
Public Version
1
Public Version Date
2022-09-30
Public Version Status
New
Public Device Record Key
b45418cf-c4be-4abc-8b15-18c282cea045

Device Description

HyFlex™ EDM Glidepath File 10/0.05 21 mm

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKS File, Pulp Canal, Endodontic

GMDN Terms

Code Name
40529 Rotary/reciprocating endodontic file/rasp, reusable

Identifiers

Type ID
Unit of Use E165600222810
Primary E165600222811

Customer Contacts

Phone
+4973458050