FDA UDI In Commercial Distribution 🇺🇸 United States

UltraTect

DI: 00883205004765 · Model: 501- · ULTRADENT PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
UltraTect
Primary DI
00883205004765
Version / Model
501-
Catalog Number
501-
Company Name
ULTRADENT PRODUCTS, INC.
Labeler DUNS
013369913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
3
Public Version Date
2020-07-07
Public Version Status
Update
Public Device Record Key
e52bd22e-853a-4b90-b2e9-75d54799b129

Device Description

Safety Glasses Clear Kit

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
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
No

Product Codes

Code Name
LYU ACCESSORY, SURGICAL APPAREL

GMDN Terms

Code Name
58376 Eye splash shield, single-use

Identifiers

Type ID
Primary 00883205004765

Customer Contacts