FDA UDI Not in Commercial Distribution 🇺🇸 United States

TO BE ASSIGNED

DI: 00999999005977 · Model: 3865003.LTS · FGX INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TO BE ASSIGNED
Primary DI
00999999005977
Version / Model
3865003.LTS
Company Name
FGX INTERNATIONAL INC.
Labeler DUNS
062312087
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-22
Public Version
3
Public Version Date
2023-12-20
Public Version Status
Update
Public Device Record Key
6520ac2b-a4d6-4e04-b255-b387dd34557a
Distribution End Date
2023-12-20

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HOI Spectacle, magnifying

GMDN Terms

Code Name
35065 Prescription spectacles

Identifiers

Type ID
Primary 00999999005977

Customer Contacts