FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653160990 · Model: FD578R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653160990
Version / Model
FD578R
Catalog Number
FD578R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-22
Public Version
1
Public Version Date
2020-04-30
Public Version Status
New
Public Device Record Key
7a2c500c-4580-4f5e-8cc6-8cf9bbdee669

Device Description

MEHDORN Applying Forceps, straight, 6", (145 mm), non-sterile, reusable, to be used with: FD552R, FD554R, FD556R, FD558R

Device Characteristics

Single Use
No
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
Yes
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
HBT APPLIER, HEMOSTATIC CLIP

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 04038653160990

Customer Contacts