FDA UDI In Commercial Distribution 🇺🇸 United States

Sontek Medical

DI: 10859758005006 · Model: A1002 Inner Pack · NextPhase Medical Devices LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sontek Medical
Primary DI
10859758005006
Version / Model
A1002 Inner Pack
Company Name
NextPhase Medical Devices LLC
Labeler DUNS
072868941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-20
Public Version
1
Public Version Date
2025-02-28
Public Version Status
New
Public Device Record Key
052f5bbd-8d5a-4436-8f7c-19e5bc763a34

Device Description

Suction Safe™ Swivel Y Inner pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
BZA Connector, Airway (Extension)

GMDN Terms

Code Name
37704 Anaesthesia breathing circuit, single-use

Identifiers

Type ID
Primary 10859758005006

Customer Contacts

Phone
508-261-0800