FDA UDI In Commercial Distribution 🇺🇸 United States

FluidFlo

DI: 00862528000319 · Model: 2500 · MED SYSTEMS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FluidFlo
Primary DI
00862528000319
Version / Model
2500
Catalog Number
2500
Company Name
MED SYSTEMS INC
Labeler DUNS
039978200
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-05
Public Version
1
Public Version Date
2023-09-13
Public Version Status
New
Public Device Record Key
086dd353-a886-4c70-8a1b-ad137d23d602

Device Description

FluidFlo Pneumatic percussor.

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWZ Percussor

GMDN Terms

Code Name
37475 Pneumatic chest percussor

Identifiers

Type ID
Primary 00862528000319

Customer Contacts

Phone
858-483-9671