FDA UDI In Commercial Distribution 🇺🇸 United States

Hollister

DI: 00610075088003 · Model: 8800 · HOLLISTER INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Hollister
Primary DI
00610075088003
Version / Model
8800
Catalog Number
8800
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
fb35a0ab-bb04-44c1-83d6-f4e95f0761d3

Device Description

Ostomy Skin Barrier, Flextend

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
EXE PROTECTOR, OSTOMY

GMDN Terms

Code Name
48159 Intestinal ostomy base plate, flat

Identifiers

Type ID
Package 20610075088007
Primary 00610075088003
Unit of Use 00610075083589

Customer Contacts

Device Sizes

Type Value Unit Text
Height 10 Centimeter
Width 10 Centimeter