FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 10810050242889 · Model: 9038 · DOMICO MED-DEVICE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
N/A
Primary DI
10810050242889
Version / Model
9038
Company Name
DOMICO MED-DEVICE, LLC
Labeler DUNS
081253414
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2020-09-24
Public Version
1
Public Version Date
2020-10-02
Public Version Status
New
Public Device Record Key
a4d35c9d-d1fd-4b49-9cb7-9b17ae02830b

Device Description

STRAP, NARROW SECURITY

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
KXJ Table, Radiologic
FMQ Restraint, Protective

GMDN Terms

Code Name
62482 Limb/torso/head restraint, reusable

Identifiers

Type ID
Unit of Use 00810050242882
Primary 10810050242889