FDA UDI In Commercial Distribution 🇺🇸 United States

Wolf-Pak

DI: 00857800006011 · Model: RF5000 · NDC HOMECARE LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Wolf-Pak
Primary DI
00857800006011
Version / Model
RF5000
Catalog Number
RF5000
Company Name
NDC HOMECARE LLC
Labeler DUNS
939966016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-13
Public Version
1
Public Version Date
2022-10-21
Public Version Status
New
Public Device Record Key
aaca16f5-023e-4a65-8e83-75456543f48b

Device Description

IV SET 20D 92" FLO REG Y 50/CS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 00857800006318
Primary 00857800006011