FDA UDI In Commercial Distribution 🇺🇸 United States

Cervix Rotterdam Applicator

DI: 08717213029323 · Model: 137250P01-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cervix Rotterdam Applicator
Primary DI
08717213029323
Version / Model
137250P01-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
cd343935-311f-4012-afd7-edb4040ed7ac

Device Description

Intrauterine tube IIIII, IU-30°, L= 20 mm, (Ti)

Device Characteristics

Single Use
No
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 Conditional
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

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

GMDN Terms

Code Name
38409 Cervical/intrauterine brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 08717213029323

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070574 000

Device Sizes

Type Value Unit Text
Device Size Text, specify
Length 20.0 Millimeter
Angle 30.0 degree

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius