FDA UDI In Commercial Distribution 🇺🇸 United States

Fibreplast®

DI: 10841962115237 · Model: RT-1882KBOS-E · Qfix
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Fibreplast®
Primary DI
10841962115237
Version / Model
RT-1882KBOS-E
Catalog Number
RT-1882KBOS-E
Company Name
Qfix
Labeler DUNS
808875397
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-12-17
Public Version
3
Public Version Date
2023-12-11
Public Version Status
Update
Public Device Record Key
ff1974fd-8c1d-4553-9938-a5e1f2318dcc

Device Description

Fibreplast 48cm Hd+Shldr BoS, 3.2mm

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
Yes
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
Unit of Use 10841962115244
Primary 10841962115237

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 3.2 Millimeter
Width 48 Centimeter