FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653294282 · Model: JK489 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AESCULAP
Primary DI
04038653294282
Version / Model
JK489
Catalog Number
JK489
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-19
Public Version
8
Public Version Date
2025-07-03
Public Version Status
Update
Public Device Record Key
6562b2ef-0fe7-42a2-8185-f88f2c441e60

Device Description

Inner Lid, basis, Standard 1/1, silver, outer length: 582 mm, outer width: 291 mm, outer heigth: 36 mm

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
FRG Wrap, sterilization

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04038653294282

Customer Contacts