FDA UDI In Commercial Distribution 🇺🇸 United States

Wearable Patch

DI: 00860008806017 · Model: Rev A · Atlas Lift Tech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Wearable Patch
Primary DI
00860008806017
Version / Model
Rev A
Company Name
Atlas Lift Tech, Inc.
Labeler DUNS
034561315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-14
Public Version
1
Public Version Date
2023-08-22
Public Version Status
New
Public Device Record Key
a41d8fe7-6a3a-47f2-abf3-9d96f81cc1ff

Device Description

A disposable patch that temporarily adheres to the patient’s sternum, allowing for the housing of the Atlas Sensor

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KMI Monitor, Bed Patient

GMDN Terms

Code Name
12391 Wearable multiple physiological parameter recorder, reusable

Identifiers

Type ID
Primary 00860008806017
Package 10860008806014
Package 20860008806011
Package 30860008806018