FDA UDI In Commercial Distribution 🇺🇸 United States

IMDK

DI: 06973912940075 · Model: C101B2 · IMDK
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IMDK
Primary DI
06973912940075
Version / Model
C101B2
Company Name
IMDK
Labeler DUNS
544547964
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-16
Public Version
1
Public Version Date
2022-05-24
Public Version Status
New
Public Device Record Key
8e573036-0c6c-4b75-b665-69b979e8bce6

Device Description

Fingertip Pulse Oximeter

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OCH Oximeter, Infrared, Sporting, Aviation

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 06973912940075