FDA UDI In Commercial Distribution 🇺🇸 United States

Cutter ejector

DI: 04250337100911 · Model: RPE280380 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cutter ejector
Primary DI
04250337100911
Version / Model
RPE280380
Catalog Number
RPE280380
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
37ca95cb-a50b-487c-9e96-165a31858dac

Device Description

Reamer Push-Ejector, green

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
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
HTO REAMER

GMDN Terms

Code Name
32579 Spinal endoscopic-access system

Identifiers

Type ID
Primary 04250337100911

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify L 280 mm / OD 3.8 mm