FDA UDI In Commercial Distribution 🇺🇸 United States

EKCOMED

DI: 00850000965140 · Model: EKM-PCB00635 · Ekcomed, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EKCOMED
Primary DI
00850000965140
Version / Model
EKM-PCB00635
Catalog Number
EKM-PCB00635
Company Name
Ekcomed, Inc.
Labeler DUNS
119213735
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-05
Public Version
1
Public Version Date
2024-11-13
Public Version Status
New
Public Device Record Key
714bfbf9-408c-45a9-a005-17342b3444d7

Device Description

Patient Boot Pad Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CCX Support, Patient Position

GMDN Terms

Code Name
44851 Limb/torso/head restraint, single-use

Identifiers

Type ID
Primary 00850000965140

Customer Contacts

Phone
800-517-1833