FDA UDI Not in Commercial Distribution 🇺🇸 United States

PURELIFE

DI: D79011901061 · Model: 1190106 · PURELIFE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
PURELIFE
Primary DI
D79011901061
Version / Model
1190106
Catalog Number
1190106
Company Name
PURELIFE, LLC
Labeler DUNS
828690904
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2017-03-17
Public Version
4
Public Version Date
2020-04-28
Public Version Status
Update
Public Device Record Key
c65ece9a-5a6f-4acb-ba88-638d5741e196
Distribution End Date
2020-04-27

Device Description

STERILIZATION POUCHES - 7-1/2" X 12"

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
Yes
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
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package D79011901063
Primary D79011901061
Unit of Use D79011901060

Customer Contacts

Phone
8777773303

Device Sizes

Type Value Unit Text
Device Size Text, specify 7-1/2" X 12"

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Cool dry place