FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 00610075062539 · Model: 19803 · HOLLISTER INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
New Image
Primary DI
00610075062539
Version / Model
19803
Catalog Number
19803
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
ec1c4f5d-4508-4626-995d-18728e3b43b3

Device Description

Colostomy/Ileostomy Kit, CeraPlus

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
62526 Urostomy bag/support kit

Identifiers

Type ID
Package 10610075062536
Primary 00610075062539
Unit of Use 20610075062533

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 44 Millimeter
Lumen/Inner Diameter 57 Millimeter