FDA UDI Not in Commercial Distribution 🇺🇸 United States

DL950 Braemar

DI: B146DL95000 · Model: 900-0616-00 · BRAEMAR MANUFACTURING, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DL950 Braemar
Primary DI
B146DL95000
Version / Model
900-0616-00
Company Name
BRAEMAR MANUFACTURING, LLC
Labeler DUNS
049529118
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-13
Public Version
5
Public Version Date
2025-08-04
Public Version Status
Update
Public Device Record Key
1f1f5b8f-5401-4c89-9392-8f08442ff8a2
Distribution End Date
2025-07-11

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWJ Electrocardiograph, Ambulatory (Without Analysis)

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary B146DL95000