FDA UDI In Commercial Distribution 🇺🇸 United States

BAM

DI: 10603354130347 · Model: REV00 · EHOB INC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BAM
Primary DI
10603354130347
Version / Model
REV00
Catalog Number
B0166B1
Company Name
EHOB INC
Labeler DUNS
150600252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-03
Public Version
2
Public Version Date
2024-09-16
Public Version Status
Update
Public Device Record Key
15d6974d-e03c-464d-8920-d8fb06b146bb

Device Description

BAM Air LC (RS/CTES) 1 Qty - Single Packed

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
Yes
MRI Safety
MR Safe
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
FSA Lift, Patient, Non-Ac-Powered

GMDN Terms

Code Name
37480 General-purpose patient lifting system sling/harness

Identifiers

Type ID
Package 30603354130334
Primary 10603354130347