FDA UDI In Commercial Distribution 🇺🇸 United States

twiist

DI: 00850017421448 · Model: DKPI-11099-001 · SEQUEL MED TECH, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
twiist
Primary DI
00850017421448
Version / Model
DKPI-11099-001
Company Name
SEQUEL MED TECH, LLC
Labeler DUNS
119070341
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-04-10
Public Version
1
Public Version Date
2025-04-18
Public Version Status
New
Public Device Record Key
acf09e61-9fe0-4aab-8998-27bb964a82a8

Device Description

twiist Disposable Cassette Pack (Sterile)

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
No
MRI Safety
MR Unsafe
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
QJI Interoperable Automated Glycemic Controller

GMDN Terms

Code Name
60770 Ambulatory insulin infusion pump/interstitial glucose monitoring system

Identifiers

Type ID
Unit of Use 00850017421431
Primary 00850017421448

Customer Contacts

Phone
877-489-4478
Phone
603-206-0591