FDA UDI In Commercial Distribution 🇺🇸 United States

Gyrus ACMI

DI: 00821925035119 · Model: 140441 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
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
Gyrus ACMI
Primary DI
00821925035119
Version / Model
140441
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
7
Public Version Date
2025-07-17
Public Version Status
Update
Public Device Record Key
b366f1ea-7b2e-442e-9d42-631fd232af2a

Device Description

NEIMAN SEPTAL SPLINT SILICONE (2/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
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
No

Product Codes

Code Name
LYA SPLINT, INTRANASAL SEPTAL

GMDN Terms

Code Name
31919 Intranasal splint, non-biodegradable

Identifiers

Type ID
Package 00821925017252
Primary 00821925035119