FDA UDI In Commercial Distribution 🇺🇸 United States

Armstrong Activent®

DI: 00681490030304 · Model: 1030170 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Armstrong Activent®
Primary DI
00681490030304
Version / Model
1030170
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-13
Public Version
4
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
9d249f7d-5eec-4a9c-a3c4-31859d12ac9d

Device Description

VENT TUBE 1030170 5PK MOD ARMSTR GROMMET

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 20681490030308
Primary 00681490030304

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K961873 000

Device Sizes

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