FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964723032 · Model: US504SU · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
AESCULAP
Primary DI
04046964723032
Version / Model
US504SU
Catalog Number
US504SU
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
9f92f493-e3e7-46b9-aa21-1d6006a163c3
Distribution End Date
2022-04-02

Device Description

SPECIALTY DISPO FCPS 203MM,0.5MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
56296 Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 04046964723032
Unit of Use 04046964723025

Customer Contacts