FDA UDI In Commercial Distribution 🇺🇸 United States

ATR+

DI: 10603354120607 · Model: REV00 · EHOB INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ATR+
Primary DI
10603354120607
Version / Model
REV00
Catalog Number
PPATR3PCCT
Company Name
EHOB INC
Labeler DUNS
150600252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-19
Public Version
1
Public Version Date
2021-03-29
Public Version Status
New
Public Device Record Key
8bdec58a-48cd-475e-9247-656d889cff24

Device Description

ATR+ Pro (RS/6 CTES/2 CWDG)

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
Yes
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
62292 Freestanding patient positioner, single-use

Identifiers

Type ID
Package 30603354120618
Primary 10603354120607