FDA UDI In Commercial Distribution 🇺🇸 United States

PERMA PURE

DI: 00840106901579 · Model: ME SERIES · PERMA PURE LLC
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
1

Basic Information

Brand Name
PERMA PURE
Primary DI
00840106901579
Version / Model
ME SERIES
Catalog Number
ME-050-03-261
Company Name
PERMA PURE LLC
Labeler DUNS
063142533
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-29
Public Version
2
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
cbd78bca-d059-417a-b4af-81090e002519

Device Description

CUSTOM ME DRYER

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
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
CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)

GMDN Terms

Code Name
45566 Gas-sampling/monitoring respiratory tubing, single-use

Identifiers

Type ID
Package 00840106901616
Primary 00840106901579
Package 00840106901609
Package 00840106901593
Package 00840106901586