FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389811337 · Model: CPRM2226FPM · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10884389811337
Version / Model
CPRM2226FPM
Catalog Number
CPRM2226FPM
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-29
Public Version
1
Public Version Date
2020-11-06
Public Version Status
New
Public Device Record Key
16a8b339-9270-4ed0-98b9-2022b7185385

Device Description

PED RESUS TUBE RES FILTER, PEEP, MANO

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BTM Ventilator, emergency, manual (resuscitator)

GMDN Terms

Code Name
57824 Resuscitator face mask, single-use

Identifiers

Type ID
Primary 10884389811337

Customer Contacts