FDA UDI In Commercial Distribution 🇺🇸 United States

Vacutron

DI: 00026072010754 · Model: 22-19-4111 · Allied Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Vacutron
Primary DI
00026072010754
Version / Model
22-19-4111
Company Name
Allied Medical, LLC
Labeler DUNS
119066872
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
5
Public Version Date
2025-10-13
Public Version Status
Update
Public Device Record Key
7f6f0ce9-e8fa-40dd-8382-4e0e5f3b9656

Device Description

Mini-Vac

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
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

GMDN Terms

Code Name
44809 Vacuum suction regulator/regulation set, general-purpose

Identifiers

Type ID
Primary 00026072010754