FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOPILOT

DI: 04038653359165 · Model: NP603P · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOPILOT
Primary DI
04038653359165
Version / Model
NP603P
Catalog Number
NP603P
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-29
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
729914b8-385a-48bf-bd94-3185b5a7fd43

Device Description

PROSTHESIS INSTRUMENTS MOLDED TRAY #2

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
62851 Surgical instrument interim-placement holder, reusable

Identifiers

Type ID
Primary 04038653359165

Customer Contacts