FDA UDI In Commercial Distribution 🇺🇸 United States

SourceMark

DI: 00897392001988 · Model: M1024 · SOURCEMARK, LLC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SourceMark
Primary DI
00897392001988
Version / Model
M1024
Company Name
SOURCEMARK, LLC.
Labeler DUNS
121225812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
5
Public Version Date
2020-07-09
Public Version Status
Update
Public Device Record Key
0ee5898a-15de-40b1-95cd-ff8d4f01ad84

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BTQ Airway, Nasopharyngeal

GMDN Terms

Code Name
42422 Nasopharyngeal airway, single-use

Identifiers

Type ID
Primary 00897392001988
Package 10897392004245
Package 20897392005430