FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964930751 · Model: US754 · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
250

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Basic Information

Brand Name
AESCULAP
Primary DI
04046964930751
Version / Model
US754
Catalog Number
US754
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
250
Record Status
Published
Publish Date
2016-09-22
Public Version
7
Public Version Date
2025-02-21
Public Version Status
Update
Public Device Record Key
93373557-49e1-4b9d-b001-91c43328e4e7

Device Description

INTERNAL PROCESS INDICATORS

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JOJ Indicator, physical/chemical sterilization process

GMDN Terms

Code Name
35362 Chemical/physical sterilization process indicator

Identifiers

Type ID
Primary 04046964930751
Unit of Use 04046964930744

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at controlled room temp
Type
Special Storage Condition, Specify