FDA UDI In Commercial Distribution 🇺🇸 United States

KOHDENT

DI: 04251436930553 · Model: 9205 · Kohdent Roland Kohler Medizintechnik GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KOHDENT
Primary DI
04251436930553
Version / Model
9205
Catalog Number
9205
Company Name
Kohdent Roland Kohler Medizintechnik GmbH & Co. KG
Labeler DUNS
324006097
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-30
Public Version
1
Public Version Date
2021-09-07
Public Version Status
New
Public Device Record Key
9b03b822-557a-4689-8887-a4a66e5324a8

Device Description

Spreader 20/30 ENDOBLACK

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
Yes
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
EIX PROBE, PERIODONTIC

GMDN Terms

Code Name
17890 Endodontic filling material condenser

Identifiers

Type ID
Primary 04251436930553

Customer Contacts