FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964969478 · Model: US899 · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964969478
Version / Model
US899
Catalog Number
US899
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-02
Public Version
2
Public Version Date
2021-05-28
Public Version Status
Update
Public Device Record Key
be2e4c2a-a3f8-4db0-ac07-bd490756fe13

Device Description

STRINGER OPEN 200 X 65MM

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
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
64168 Sterilization stringer

Identifiers

Type ID
Primary 04046964969478

Customer Contacts