FDA UDI In Commercial Distribution 🇺🇸 United States

VERESS

DI: 04048223077498 · Model: 1206-00150 · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VERESS
Primary DI
04048223077498
Version / Model
1206-00150
Catalog Number
1206-00150
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-02
Public Version
2
Public Version Date
2021-07-08
Public Version Status
Update
Public Device Record Key
5ed40429-faef-451e-aa43-7bc1efd652ad

Device Description

1206-00150

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HET LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

GMDN Terms

Code Name
46329 Spring-loaded pneumoperitoneum needle, reusable

Identifiers

Type ID
Previous 04048223008331
Primary 04048223077498

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 65 Percent (%) Relative Humidity