FDA UDI In Commercial Distribution 🇺🇸 United States

Crosstex International

DI: 10732224109296 · Model: SCL10152 · CROSSTEX INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Crosstex International
Primary DI
10732224109296
Version / Model
SCL10152
Catalog Number
SCL10152
Company Name
CROSSTEX INTERNATIONAL, INC.
Labeler DUNS
057728685
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-11-11
Public Version
5
Public Version Date
2023-08-31
Public Version Status
Update
Public Device Record Key
166c2ab1-a64d-4691-80b5-5a5f5275ac70

Device Description

(SURE CHECK 10X15 POUCH)

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 50732224109294
Primary 10732224109296
Unit of Use 00732224109299

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K941327 000