FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046955920341 · Model: US985SU · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

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Basic Information

Brand Name
AESCULAP
Primary DI
04046955920341
Version / Model
US985SU
Catalog Number
US985SU
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2025-10-31
Public Version
1
Public Version Date
2025-11-10
Public Version Status
New
Public Device Record Key
eebb9bf6-4395-44c6-aa7e-3e7bba3c145a

Device Description

SPECIALTY IRR DISP FCP 203 X 76 X 1.0 MM

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
Unit of Use 04046955920334
Primary 04046955920341

Customer Contacts