FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6333974370 · Model: 39-7437 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M6333974370
Version / Model
39-7437
Catalog Number
39-7437
Company Name
JEDMED INSTRUMENT COMPANY
Labeler DUNS
092987189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-03
Public Version
1
Public Version Date
2023-02-13
Public Version Status
New
Public Device Record Key
578b38e3-14fa-4b5a-b150-cfa243cb91c4

Device Description

FOOTSWITCH F/HORUS SCOPE

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
No
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
HKI Camera, Ophthalmic, Ac-Powered

GMDN Terms

Code Name
36739 Camera control unit

Identifiers

Type ID
Primary M6333974370

Premarket Submissions

Submission Number Supplement Number
K120982 000