FDA UDI In Commercial Distribution 🇺🇸 United States

DermaDam

DI: 00883205015891 · Model: 314- · ULTRADENT PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DermaDam
Primary DI
00883205015891
Version / Model
314-
Catalog Number
314-
Company Name
ULTRADENT PRODUCTS, INC.
Labeler DUNS
013369913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-01
Public Version
1
Public Version Date
2018-10-02
Public Version Status
New
Public Device Record Key
a4c729b9-f7de-4247-8331-f52a42331af4

Device Description

DermaDam Heavy 36pk

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
EIE DAM, RUBBER

GMDN Terms

Code Name
11155 Rubber dam, Hevea-latex

Identifiers

Type ID
Primary 00883205015891

Customer Contacts