FDA UDI In Commercial Distribution 🇺🇸 United States

TOPCARE

DI: 00036800023420 · Model: 52-50K · TOPCO ASSOCIATES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TOPCARE
Primary DI
00036800023420
Version / Model
52-50K
Company Name
TOPCO ASSOCIATES, LLC
Labeler DUNS
072943876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-04
Public Version
2
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
3db3284c-f0c9-49a1-a14e-6fa7e5d9222c

Device Description

TOPCARE 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
No
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
DQA Oximeter

GMDN Terms

Code Name
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Package 10036800023427
Primary 00036800023420

Customer Contacts