FDA UDI In Commercial Distribution 🇺🇸 United States

Self-Sealing Sterilization Bag

DI: 30732224001129 · Model: OC · CROSSTEX INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1000

Basic Information

Brand Name
Self-Sealing Sterilization Bag
Primary DI
30732224001129
Version / Model
OC
Company Name
CROSSTEX INTERNATIONAL, INC.
Labeler DUNS
057728685
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2022-05-03
Public Version
2
Public Version Date
2023-12-29
Public Version Status
Update
Public Device Record Key
ce7ed4c5-8a30-4f48-8836-23dd2a8a5f17

Device Description

Self-Sealing Sterilization Bag,2.5 in x 1.5 in x 10.5 in (6.5 cm x 4 cm x 27 cm)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
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 50732224001123
Primary 30732224001129
Unit of Use 00732224001128

Customer Contacts