FDA UDI Not in Commercial Distribution 🇺🇸 United States

Denco

DI: 06970514919065 · Model: 21mm Super fileIII(Engine) F2 · SHENZHEN DENCO MEDICAL CO., LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Denco
Primary DI
06970514919065
Version / Model
21mm Super fileIII(Engine) F2
Company Name
SHENZHEN DENCO MEDICAL CO., LTD
Labeler DUNS
543035008
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-25
Public Version
1
Public Version Date
2023-10-03
Public Version Status
New
Public Device Record Key
4633093f-253d-40ae-90de-cc8176dd1f95
Distribution End Date
2023-09-26

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
EKS File, Pulp Canal, Endodontic

GMDN Terms

Code Name
63550 Rotary/reciprocating endodontic file/rasp, single-use

Identifiers

Type ID
Primary 06970514919065