FDA UDI In Commercial Distribution 🇺🇸 United States

Diversatek Healthcare

DI: 00816734021835 · Model: A86-4300-10 · DIVERSATEK HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Diversatek Healthcare
Primary DI
00816734021835
Version / Model
A86-4300-10
Catalog Number
A86-4300-10
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-30
Public Version
1
Public Version Date
2023-07-10
Public Version Status
New
Public Device Record Key
2cbe67cc-6543-4417-98b8-dcacebf96a3a

Device Description

Anorectal Balloon, 400CC TPE

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
FFX System, Gastrointestinal Motility (Electrical)

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system

Identifiers

Type ID
Package 10816734021832
Primary 00816734021835
Secondary B019A864300100

Customer Contacts

Phone
800-558-6408