FDA UDI In Commercial Distribution 🇺🇸 United States

Tresident 2000 K

DI: ESDG2120101 · Model: 212010 · Schütz Dental GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Tresident 2000 K
Primary DI
ESDG2120101
Version / Model
212010
Company Name
Schütz Dental GmbH
Labeler DUNS
315830349
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-13
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
95ca7ae7-8540-4812-a296-0505e0028f18

Device Description

Workable, addition-cross linking precision impression material based on vinylpolysilox.

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
No
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
No

Product Codes

Code Name
ELW Material, Impression

GMDN Terms

Code Name
35866 Silicone dental impression material

Identifiers

Type ID
Primary ESDG2120101

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
18 – 25 Degrees Celsius