FDA UDI In Commercial Distribution 🇺🇸 United States

ErgoTube

DI: 04048223007501 · Model: 1292-14-10 · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ErgoTube
Primary DI
04048223007501
Version / Model
1292-14-10
Catalog Number
1292-14-10
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-08
Public Version
2
Public Version Date
2021-03-16
Public Version Status
Update
Public Device Record Key
ee5f7a2b-5740-4fa0-97cf-e6a2f9d4ce23
Distribution End Date
2025-03-15

Device Description

ErgoTube 10mm shaft isolated 450mm long, adaptabl to all handles and instrument-inserts

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
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
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
33596 Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

Identifiers

Type ID
Primary 04048223007501

Customer Contacts