FDA UDI In Commercial Distribution 🇺🇸 United States

Dentrix

DI: 00618125126262 · Model: 20954 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dentrix
Primary DI
00618125126262
Version / Model
20954
Catalog Number
6148998
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-07
Public Version
1
Public Version Date
2022-10-17
Public Version Status
New
Public Device Record Key
1acfffea-c0f0-4adc-a397-ae157751cdc7

Device Description

XIOS Plus Hygienic Covers Size 1

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQM Camera, Surgical And Accessories

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Package 10618125126269
Primary 00618125126262