FDA UDI In Commercial Distribution 🇺🇸 United States

Edge™ EarLoop Procedure Masks

DI: 10818365020949 · Model: 5722008 · EDGE ENDO LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Edge™ EarLoop Procedure Masks
Primary DI
10818365020949
Version / Model
5722008
Catalog Number
5722008
Company Name
EDGE ENDO LLC
Labeler DUNS
078474365
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-02-06
Public Version
2
Public Version Date
2020-05-06
Public Version Status
Update
Public Device Record Key
278f3cb9-e15e-4afd-9ada-ea5f1dc9a9d1

Device Description

Earloop Procedure Masks, ASTM Level 1, Pink, Box

Device Characteristics

Single Use
Yes
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
FXX Mask, Surgical

GMDN Terms

Code Name
35177 Surgical/medical face mask, single-use

Identifiers

Type ID
Primary 10818365020949
Unit of Use 00818365020942
Package 20818365020946

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
– 40 Degrees Celsius