FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964910463 · Model: US992 · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1000

Basic Information

Brand Name
AESCULAP
Primary DI
04046964910463
Version / Model
US992
Catalog Number
US992
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
1f1cdcb8-03d7-4761-baba-b79419d9a4a1

Device Description

QUARTER-SIZE FILTERS

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
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
60909 Sterilization container filter, single-use

Identifiers

Type ID
Primary 04046964910463
Unit of Use 04046964910456

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place
Type
Special Storage Condition, Specify
Special Conditions
Avoid extreme temperature
Type
Special Storage Condition, Specify
Special Conditions
Store in a cool place