FDA UDI In Commercial Distribution 🇺🇸 United States

Medichoice

DI: 10885632101533 · Model: HR1000 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medichoice
Primary DI
10885632101533
Version / Model
HR1000
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-20
Public Version
6
Public Version Date
2023-11-27
Public Version Status
Update
Public Device Record Key
7cf7c99c-cbda-48ab-aae0-18f64077088e

Device Description

Pouch Sterilization Heat-Seal Ethylene Oxide Steam Dual Indicator Blue-Tinted Kraft Paper 100 Feet 10 Inch Not Made With Natural Rubber Latex MediChoice

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FRG Wrap, sterilization

GMDN Terms

Code Name
60908 Sterilization container liner

Identifiers

Type ID
Package 50885632101531
Primary 10885632101533

Premarket Submissions

Submission Number Supplement Number
K112591 000

Device Sizes

Type Value Unit Text
Width 10 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid Direct Sunlight, Avoid Rain
Type
Special Storage Condition, Specify