FDA UDI In Commercial Distribution 🇺🇸 United States

KMEDIC

DI: 24026704288285 · Model: IPN015383 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KMEDIC
Primary DI
24026704288285
Version / Model
IPN015383
Catalog Number
KM56174
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-15
Public Version
2
Public Version Date
2021-01-18
Public Version Status
Update
Public Device Record Key
e357bed4-f6ad-4e43-a092-9bf7b23a2a6e

Device Description

GRUBER EAR SPECULUM ADULT # 3 CHROME

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EPY SPECULUM, ENT

GMDN Terms

Code Name
33395 Ear speculum, reusable

Identifiers

Type ID
Primary 24026704288285
Direct Marking 04026704288281

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult Size 4
Length 4 Centimeter