FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964580390 · Model: US153SU · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AESCULAP
Primary DI
04046964580390
Version / Model
US153SU
Catalog Number
US153SU
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2020-01-15
Public Version Status
Update
Public Device Record Key
7173e87c-7624-428b-ac02-3f4e54533645

Device Description

RUSSIAN Tissue Forceps, 12", (305 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
Primary 04046964580390
Unit of Use 04046964580383

Customer Contacts