FDA UDI In Commercial Distribution 🇺🇸 United States

PRIMOBoot II - Standard

DI: 00810006683578 · Model: PBII · PRIMO INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRIMOBoot II - Standard
Primary DI
00810006683578
Version / Model
PBII
Catalog Number
PBII
Company Name
PRIMO INC
Labeler DUNS
958758146
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-21
Public Version
1
Public Version Date
2021-07-29
Public Version Status
New
Public Device Record Key
d71f589f-febc-436e-af4b-ce553ecb45ad

Device Description

PBII PRIMOBoot II - Standard 13/each

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
Yes
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
FMP Protector, Skin Pressure

GMDN Terms

Code Name
42501 Heel protector

Identifiers

Type ID
Package 10810006683575
Primary 00810006683578