FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6330358280 · Model: 03-5828 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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
JEDMED
Primary DI
M6330358280
Version / Model
03-5828
Catalog Number
03-5828
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
1
Public Version Date
2020-09-09
Public Version Status
New
Public Device Record Key
01945892-1e69-4f7f-9a75-eac6542b3f52

Device Description

INSTRUMENT DRAWER LINER F/SPECTRUM

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
ETF Unit, Examining/Treatment, Ent

GMDN Terms

Code Name
44380 ENT cabinet

Identifiers

Type ID
Primary M6330358280