FDA UDI In Commercial Distribution 🇺🇸 United States

PureFlo

DI: 00816734021453 · Model: 1195-21 · DIVERSATEK HEALTHCARE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PureFlo
Primary DI
00816734021453
Version / Model
1195-21
Catalog Number
1195-21
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-06
Public Version
1
Public Version Date
2023-07-14
Public Version Status
New
Public Device Record Key
298601fb-fae0-4334-9e8b-dcb9af6c9e7f

Device Description

PureFlo Single-Use Auxiliary Water Jet Connector

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCX Endoscopic Irrigation/Suction System
FEQ Pump, Air, Non-Manual, For Endoscope

GMDN Terms

Code Name
46102 Surgical irrigation tubing set, single-use

Identifiers

Type ID
Package 10816734021450
Primary 00816734021453

Customer Contacts

Phone
800-558-6408