FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M633301705010 · Model: 30-1705 01 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M633301705010
Version / Model
30-1705 01
Catalog Number
30-1705 01
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
286fdb51-451f-46e2-9899-f468130a09a2

Device Description

NEEDLE HOUSE STRONG LONG CURVE

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
Yes
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
LRC Instrument, Ent Manual Surgical

GMDN Terms

Code Name
13039 Middle ear pick

Identifiers

Type ID
Primary M633301705010