FDA UDI In Commercial Distribution 🇺🇸 United States

Epimed

DI: 00818788021908 · Model: 412-CCET · EPIMED INTERNATIONAL, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Epimed
Primary DI
00818788021908
Version / Model
412-CCET
Catalog Number
412-CCET
Company Name
EPIMED INTERNATIONAL, INC
Labeler DUNS
799751953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-27
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e5b3ed45-9689-4e1b-b97a-050c0ef6123a

Device Description

PainBlocker™ Console Exhaust Tubing

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXH DEVICE, SURGICAL, CRYOGENIC

GMDN Terms

Code Name
56300 Liquid nitrous oxide coaxial tubing

Identifiers

Type ID
Primary 00818788021908

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit