FDA UDI In Commercial Distribution 🇺🇸 United States

BAM

DI: 10603354130163 · Model: REV00 · EHOB INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BAM
Primary DI
10603354130163
Version / Model
REV00
Catalog Number
A0163A1
Company Name
EHOB INC
Labeler DUNS
150600252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-01
Public Version
1
Public Version Date
2024-05-09
Public Version Status
New
Public Device Record Key
c82c9991-9b29-4d6d-b65e-4a2a69f85ce1

Device Description

BAM Pro XL Repositioning Sheet – 1 ea

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
Yes
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
FMR Device, Transfer, Patient, Manual

GMDN Terms

Code Name
37163 Patient transfer sliding mat

Identifiers

Type ID
Primary 10603354130163
Package 30603354130105