FDA UDI In Commercial Distribution 🇺🇸 United States

Tub Pad

DI: 00810006681345 · Model: BP01 · PRIMO INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tub Pad
Primary DI
00810006681345
Version / Model
BP01
Catalog Number
BP01
Company Name
PRIMO INC
Labeler DUNS
958758146
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-20
Public Version
1
Public Version Date
2019-03-11
Public Version Status
New
Public Device Record Key
38881fb5-3964-4bde-989b-f4e4acdb8566

Device Description

Tub Pad

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
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
58878 Freestanding patient positioner, reusable

Identifiers

Type ID
Primary 00810006681345