FDA UDI In Commercial Distribution 🇺🇸 United States

EKCOMED

DI: 00850000965072 · Model: EKM-MCP401 · Ekcomed, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
EKCOMED
Primary DI
00850000965072
Version / Model
EKM-MCP401
Catalog Number
EKM-MCP401
Company Name
Ekcomed, Inc.
Labeler DUNS
119213735
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-10-27
Public Version
3
Public Version Date
2024-11-06
Public Version Status
Update
Public Device Record Key
4936dab6-88bc-4367-b473-2f5ff0359232

Device Description

McPull Shoulder 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
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

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

Identifiers

Type ID
Primary 00850000965072
Unit of Use 10850000965079

Customer Contacts

Phone
800-517-1833