FDA UDI In Commercial Distribution 🇺🇸 United States

Optiband Ultra

DI: 00889989075434 · Model: 740-0295 · ORMCO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Optiband Ultra
Primary DI
00889989075434
Version / Model
740-0295
Company Name
ORMCO CORPORATION
Labeler DUNS
154614119
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-12-06
Public Version
1
Public Version Date
2022-12-14
Public Version Status
New
Public Device Record Key
d9d9faf0-f7b9-432f-bb04-b5a854b94eb4

Device Description

OPTIBAND TIP REFILL KIT PK50

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DYH ADHESIVE, BRACKET AND TOOTH CONDITIONER, RESIN

GMDN Terms

Code Name
35697 Dental material application tool, single-use

Identifiers

Type ID
Unit of Use 10889989075431
Primary 00889989075434

Customer Contacts

Phone
+18008541741