FDA UDI In Commercial Distribution 🇺🇸 United States

PUSHER

DI: 04260647240214 · Model: KR-0200 · Morpheus AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PUSHER
Primary DI
04260647240214
Version / Model
KR-0200
Company Name
Morpheus AG
Labeler DUNS
315142027
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-28
Public Version
1
Public Version Date
2022-07-06
Public Version Status
New
Public Device Record Key
b261676b-d900-486d-9f31-8550c6a80c2f

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
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
34878 Surgical instrument/endoscope cleaning utensil, reusable

Identifiers

Type ID
Primary 04260647240214