FDA UDI In Commercial Distribution 🇺🇸 United States

SourceMark

DI: 00813799003127 · Model: M0365 · SOURCEMARK, LLC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SourceMark
Primary DI
00813799003127
Version / Model
M0365
Company Name
SOURCEMARK, LLC.
Labeler DUNS
121225812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-08
Public Version
1
Public Version Date
2020-07-16
Public Version Status
New
Public Device Record Key
eb693687-5de9-4dac-9100-32c9b3e0bc94

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
CAE Airway, Oropharyngeal, Anesthesiology

GMDN Terms

Code Name
45036 Laryngeal mask airway, single-use

Identifiers

Type ID
Package 10813799003131
Primary 00813799003127
Package 20813799003145