FDA UDI Not in Commercial Distribution 🇺🇸 United States

EndoRotor® 2550 Catheter

DI: 00865830000268 · Model: ER 10-02 · INTERSCOPE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndoRotor® 2550 Catheter
Primary DI
00865830000268
Version / Model
ER 10-02
Catalog Number
ER 10-02
Company Name
INTERSCOPE, INC
Labeler DUNS
968227913
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-02
Public Version
2
Public Version Date
2024-02-12
Public Version Status
Update
Public Device Record Key
3b8e50e0-fddf-4a04-ad14-1bc191dfbac4
Distribution End Date
2023-01-01

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PTE Endoscopic Morcellator Gastroenterology

GMDN Terms

Code Name
46732 Tissue morcellation system handpiece, line-powered

Identifiers

Type ID
Primary 00865830000268

Customer Contacts