FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6333816500 · Model: 38-1650 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M6333816500
Version / Model
38-1650
Catalog Number
38-1650
Company Name
JEDMED INSTRUMENT COMPANY
Labeler DUNS
092987189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-08
Public Version
1
Public Version Date
2023-05-16
Public Version Status
New
Public Device Record Key
5e91ce14-142a-49fe-8910-bd58c0f8b035

Device Description

U-Tube 1.35mm ID

Device Characteristics

Single Use
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
ETD Tube, Tympanostomy

GMDN Terms

Code Name
33794 Tympanostomy tube

Identifiers

Type ID
Primary M6333816500