FDA UDI In Commercial Distribution 🇺🇸 United States

Ethox

DI: 20889483149994 · Model: 950093500 · ETHOX MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ethox
Primary DI
20889483149994
Version / Model
950093500
Catalog Number
950093500
Company Name
ETHOX MEDICAL, LLC
Labeler DUNS
079149179
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-21
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
3f7d5fb2-a75c-4ea9-85e5-5c038ae2113a

Device Description

ETHOX LK-700N LAP 2 POCKET W/TAPE - NS

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
12236 Surgical instrument interim-placement holder, single-use

Identifiers

Type ID
Primary 20889483149994

Customer Contacts

Device Sizes

Type Value Unit Text
Width 28 Centimeter