FDA UDI In Commercial Distribution 🇺🇸 United States

Prometheus Omni Splint Rolled

DI: 05060483570099 · Model: PDF105 · SAFEGUARD MEDICAL TECHNOLOGIES LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prometheus Omni Splint Rolled
Primary DI
05060483570099
Version / Model
PDF105
Catalog Number
PDF105
Company Name
SAFEGUARD MEDICAL TECHNOLOGIES LIMITED
Labeler DUNS
219545612
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-04
Public Version
1
Public Version Date
2023-05-12
Public Version Status
New
Public Device Record Key
2ee6af35-5a30-4848-b5e5-7f11f2b7e92d
Distribution End Date
2030-05-04

Device Description

The Prometheus Omni Splint™ is intended to be used to aid support and immobilize a patient’s limb(s).

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile

GMDN Terms

Code Name
64881 First aid limb splint, mouldable, single-use

Identifiers

Type ID
Primary 05060483570099