FDA UDI Not in Commercial Distribution 🇺🇸 United States

Domico Med-Device

DI: 00810050240116 · Model: 430-UF · DOMICO MED-DEVICE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Domico Med-Device
Primary DI
00810050240116
Version / Model
430-UF
Company Name
DOMICO MED-DEVICE, LLC
Labeler DUNS
081253414
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-10
Public Version
2
Public Version Date
2023-02-22
Public Version Status
Update
Public Device Record Key
d9e71457-6adb-46ef-ac79-76a12d5b6cd1
Distribution End Date
2023-02-17

Device Description

BLOCK, DUAL OBLIQUE HAND

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
No

Product Codes

Code Name
CCX Support, Patient Position

GMDN Terms

Code Name
41058 Multifunction body cushion

Identifiers

Type ID
Primary 00810050240116