FDA UDI In Commercial Distribution 🇺🇸 United States

Rotterdam Nasopharyngeal Mold

DI: 08717213010109 · Model: 089062-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rotterdam Nasopharyngeal Mold
Primary DI
08717213010109
Version / Model
089062-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
13e2a0d3-f4f6-4b0c-b048-f997806589b7

Device Description

Rotterdam Nasopharynx Mold Applicator

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JAQ System, applicator, radionuclide, remote-controlled

GMDN Terms

Code Name
38415 Nasopharynx brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 08717213010109

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K983337 000