FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6330355550 · Model: 03-5555 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
JEDMED
Primary DI
M6330355550
Version / Model
03-5555
Catalog Number
03-5555
Company Name
JEDMED INSTRUMENT COMPANY
Labeler DUNS
092987189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-13
Public Version
1
Public Version Date
2018-08-13
Public Version Status
New
Public Device Record Key
11bf0128-38e0-4bf1-9de1-f4f8bf651d79

Device Description

Conversion Kit /Glass Trap

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
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
38476 Suction system bottle

Identifiers

Type ID
Primary M6330355550

Customer Contacts

Phone
314-845-3770