FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6333988000 · Model: 39-8800 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M6333988000
Version / Model
39-8800
Catalog Number
39-8800
Company Name
JEDMED INSTRUMENT COMPANY
Labeler DUNS
092987189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-01
Public Version
2
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
22e319df-c6c4-4517-80e9-1dfac0fa1bd2

Device Description

GENERAL VIEWING LENS

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
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
ERA Otoscope

GMDN Terms

Code Name
12849 Otoscope, direct

Identifiers

Type ID
Primary M6333988000