FDA UDI In Commercial Distribution 🇺🇸 United States

Premier

DI: 00610075890019 · Model: 89001 · HOLLISTER INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Premier
Primary DI
00610075890019
Version / Model
89001
Catalog Number
89001
Company Name
HOLLISTER INCORPORATED
Labeler DUNS
005527098
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
6dc39782-9296-4e62-a9b7-1e0b9dde9213

Device Description

Colostomy/Ileostomy Kit, SoftFlex

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
No
PM Exempt
Yes
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
PQE Ostomy care kit

GMDN Terms

Code Name
62525 Intestinal ostomy bag/support kit

Identifiers

Type ID
Package 10610075890016
Primary 00610075890019
Unit of Use 20610075890013

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 64 Millimeter