FDA UDI In Commercial Distribution 🇺🇸 United States

Crosstex™ Isolator™ Molded N95 Surgical Respirator

DI: 10732224004690 · Model: GMLRESP · CROSSTEX INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Crosstex™ Isolator™ Molded N95 Surgical Respirator
Primary DI
10732224004690
Version / Model
GMLRESP
Company Name
CROSSTEX INTERNATIONAL, INC.
Labeler DUNS
057728685
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2021-06-14
Public Version
4
Public Version Date
2023-09-13
Public Version Status
Update
Public Device Record Key
d5eb3973-1cdf-4ced-9dd9-3c3c25c4553a

Device Description

Surgical Respirator

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MSH Respirator, surgical

GMDN Terms

Code Name
57794 Surgical/medical respirator, non-antimicrobial, single-use

Identifiers

Type ID
Package 50732224004698
Primary 10732224004690
Unit of Use 00732224004693

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061375 000