FDA UDI In Commercial Distribution 🇺🇸 United States

Ultrapak

DI: 00883205003805 · Model: 132 · ULTRADENT PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ultrapak
Primary DI
00883205003805
Version / Model
132
Catalog Number
132
Company Name
ULTRADENT PRODUCTS, INC.
Labeler DUNS
013369913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-28
Public Version
1
Public Version Date
2018-05-29
Public Version Status
New
Public Device Record Key
0aa8531f-adec-4962-bd58-37594ea9ea4b

Device Description

Ultrapak Cord #1

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JES FLOSS, DENTAL

GMDN Terms

Code Name
35861 Gingival retraction cord, non-medicated

Identifiers

Type ID
Primary 00883205003805

Customer Contacts