FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6330355500 · Model: 03-5550 · 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
M6330355500
Version / Model
03-5550
Catalog Number
03-5550
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
3
Public Version Date
2025-09-24
Public Version Status
Update
Public Device Record Key
714857a8-007d-44ee-a3c8-cfb31fcd63f1

Device Description

Pressure Kit F/ Classic Cabinet

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
35457 Therapeutic agent nebulizer, benchtop

Identifiers

Type ID
Primary M6330355500

Customer Contacts

Phone
314-845-3770