FDA UDI Not in Commercial Distribution 🇺🇸 United States

Aquaplast RT™

DI: 10841962102909 · Model: RT-1778ORF5 · Qfix
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Aquaplast RT™
Primary DI
10841962102909
Version / Model
RT-1778ORF5
Catalog Number
RT-1778ORF5
Company Name
Qfix
Labeler DUNS
808875397
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-12-22
Public Version
5
Public Version Date
2023-12-11
Public Version Status
Update
Public Device Record Key
fa70502c-6cce-446d-a24d-a97f11236cb5
Distribution End Date
2017-01-12

Device Description

Aquaplast Orfit 5-Point, 2.4mm

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
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, linear, medical

GMDN Terms

Code Name
40896 Patient positioning thermoplastic mould material

Identifiers

Type ID
Primary 10841962102909
Unit of Use 10841962102916

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 2.4 Millimeter