FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653052578 · Model: OK434R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653052578
Version / Model
OK434R
Catalog Number
OK434R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
3
Public Version Date
2023-08-28
Public Version Status
Update
Public Device Record Key
21ff1f74-6336-4ff8-bc40-855ae5dfc95f

Device Description

LUC Septum Forceps, 8", (200 mm), fenestrated, non-sterile, reusable

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
KAE FORCEPS, ENT

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 04038653052578

Customer Contacts