FDA UDI Not in Commercial Distribution 🇺🇸 United States

EXMOOR

DI: 05060180255848 · Model: E.1006 · EXMOOR PLASTICS LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EXMOOR
Primary DI
05060180255848
Version / Model
E.1006
Catalog Number
E.1006
Company Name
EXMOOR PLASTICS LIMITED
Labeler DUNS
298725490
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-20
Public Version
3
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
daddf905-213f-4ead-9c44-f972bdc2e5d7
Distribution End Date
2019-08-27

Device Description

Aural Grommet

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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 05060180251369
Primary 05060180255848

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K911580 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep out of direct sunlight.
Type
Storage Environment Temperature
Temperature Range
10 – 35 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Store in a dry environment. Avoid extremes of temperature and humidity.