FDA UDI In Commercial Distribution 🇺🇸 United States

Cinch™

DI: 10810000524003 · Model: S435 · PARKELL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Cinch™
Primary DI
10810000524003
Version / Model
S435
Catalog Number
S435
Company Name
PARKELL, INC.
Labeler DUNS
009900424
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2018-10-19
Public Version
3
Public Version Date
2023-01-09
Public Version Status
Update
Public Device Record Key
d3679c7a-4484-4b90-8122-74b6f9bf146f

Device Description

Cinch™-Platinum Tubes (Contains: 2-Tubes Base & 2-Tubes Cata

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 10810000524003
Unit of Use 00810000524006

Customer Contacts

Phone
6312491134

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Excessive heat will shorten shelf-life. After initial use, store in a cool, dark place with cap tightly screwed on.
Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius