FDA UDI In Commercial Distribution 🇺🇸 United States

PLUS

DI: 00810050860680 · Model: P7202-01-004 · LIFEPORT, LLC
Product Codes
4
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PLUS
Primary DI
00810050860680
Version / Model
P7202-01-004
Company Name
LIFEPORT, LLC
Labeler DUNS
556196210
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-11
Public Version
2
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
18bc6285-099e-4eb9-bc92-1d2a9432d2b2

Device Description

PLUS, 66 IN BAY WITH 6 IN CANTILEVER STRUCTURE

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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FOX Stand, Infusion
BTI Compressor, Air, Portable
CAN Regulator, Pressure, Gas Cylinder
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

GMDN Terms

Code Name
31253 Medical device air compressor
43438 Non-fixed medical gas cylinder regulator
58008 Laboratory pump, vacuum
60489 Ambulance stretcher docking device

Identifiers

Type ID
Primary 00810050860680

Customer Contacts

Phone
360-225-1212