FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046955325054 · Model: MN217R · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046955325054
Version / Model
MN217R
Catalog Number
MN217R
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-20
Public Version
1
Public Version Date
2020-07-28
Public Version Status
New
Public Device Record Key
f98fc783-aec2-4dad-b635-8b962f804ded

Device Description

CLOSED END KNOT PUSHER 5MM 400MM

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
No
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
HCF INSTRUMENT, LIGATURE PASSING AND KNOT TYING

GMDN Terms

Code Name
45716 Suture knot pusher, reusable

Identifiers

Type ID
Primary 04046955325054

Customer Contacts