FDA UDI In Commercial Distribution 🇺🇸 United States

Aquaplast RT™

DI: 10841962111185 · Model: RT-1782BOS-DXS · Qfix
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aquaplast RT™
Primary DI
10841962111185
Version / Model
RT-1782BOS-DXS
Catalog Number
RT-1782BOS-DXS
Company Name
Qfix
Labeler DUNS
808875397
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-26
Public Version
4
Public Version Date
2023-12-11
Public Version Status
Update
Public Device Record Key
9d31e529-9a5b-4fda-90d6-1dffe324277c

Device Description

Aquaplast RT 24 cm (Extra Small) Head & Neck, 2.4mm, Standard Perf

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 10841962111185

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 2.4 Millimeter