FDA UDI In Commercial Distribution 🇺🇸 United States

Armstrong Activent®

DI: 00681490029599 · Model: 1026140 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Armstrong Activent®
Primary DI
00681490029599
Version / Model
1026140
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-17
Public Version
4
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
3bd5168a-6008-4f57-9473-cf1215102c96

Device Description

VENT TUBE 1026140 ACTIVENT 5PK ARMST BEV

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 Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ETD TUBE, TYMPANOSTOMY

GMDN Terms

Code Name
33794 Tympanostomy tube

Identifiers

Type ID
Package 20681490029593
Primary 00681490029599

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K941407 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Inner Diameter is 1.14 MM
Length 7.0 Millimeter