FDA UDI In Commercial Distribution 🇺🇸 United States

Spex

DI: 09420051700970 · Model: 1405-6222-027 · SPEX LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spex
Primary DI
09420051700970
Version / Model
1405-6222-027
Catalog Number
1405-6222-027
Company Name
SPEX LIMITED
Labeler DUNS
748649195
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-12
Public Version
3
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
d458be54-578e-4914-a336-2d6909171cc5

Device Description

Spex 2-point hip belt, padded-dual centre pull with side release buckle Medium

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
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
FMQ Restraint, Protective

GMDN Terms

Code Name
13356 Wheelchair/chair/stander occupant restraint/support

Identifiers

Type ID
Primary 09420051700970

Customer Contacts

Phone
6433079790