FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964790102 · Model: MD575 · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964790102
Version / Model
MD575
Catalog Number
MD575
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-30
Public Version
6
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
a9cbeb1b-931b-4432-9193-b6d1add60b20

Device Description

CURETTE 230MM TRAY LID F 1/2SZ CONTAIN

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 04046964790102

Customer Contacts