FDA UDI Not in Commercial Distribution 🇺🇸 United States

Gyrus ACMI

DI: 00821925032644 · Model: 70140397 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

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
Gyrus ACMI
Primary DI
00821925032644
Version / Model
70140397
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2024-07-24
Public Version
3
Public Version Date
2026-04-27
Public Version Status
Update
Public Device Record Key
73820783-751f-493f-9c6e-06a4b0a26f5c
Distribution End Date
2026-03-18

Device Description

ARMSTRONG V TYPE GROMMET BLUE 1.14 MM ID FLUOROPLASTIC PACIFIC TWIN PACK (60/PK)

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
Labeling does not contain MRI Safety Information
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
ETD Tube, Tympanostomy

GMDN Terms

Code Name
33794 Tympanostomy tube

Identifiers

Type ID
Package 00821925020214
Primary 00821925032644
Unit of Use 80821925032640

Premarket Submissions

Submission Number Supplement Number
K000801 000