FDA UDI In Commercial Distribution 🇺🇸 United States

OSSEOUS Myringotomy Kit-Standard

DI: 08906039319729 · Model: EI0972 · EON MEDITECH PRIVATE LIMITED
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
OSSEOUS Myringotomy Kit-Standard
Primary DI
08906039319729
Version / Model
EI0972
Company Name
EON MEDITECH PRIVATE LIMITED
Labeler DUNS
930270428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-04
Public Version
1
Public Version Date
2024-07-12
Public Version Status
New
Public Device Record Key
ed490218-2e6c-47bd-9211-722e59509767

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 08904428747450
Primary 08906039319729

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 25 Degrees Celsius