FDA UDI In Commercial Distribution 🇺🇸 United States

Optiview

DI: 00889989059991 · Model: 716-0052 · ORMCO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Optiview
Primary DI
00889989059991
Version / Model
716-0052
Company Name
ORMCO CORPORATION
Labeler DUNS
154614119
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-09
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
86c2e03c-ffdf-4ad4-961a-18424a7771cb

Device Description

OPTIVIEW REFILL CUSHION 10PK

Device Characteristics

Single Use
Yes
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
EIG RETRACTOR, ALL TYPES

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Unit of Use 20889989059995
Primary 00889989059991

Customer Contacts

Phone
+18008541741