FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6335851750 · Model: 58-5175 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M6335851750
Version / Model
58-5175
Catalog Number
58-5175
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
d44b04ea-fb34-4a58-a5da-8221c321b787

Device Description

CRUSHER CARTILAGE

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
32873 Surgical tamp, reusable

Identifiers

Type ID
Primary M6335851750