FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653209538 · Model: OK503R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653209538
Version / Model
OK503R
Catalog Number
OK503R
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
3
Public Version Date
2023-08-24
Public Version Status
Update
Public Device Record Key
0bbf36e7-09c1-42aa-bec6-e88807104152

Device Description

HENCKEL-TILLEYS Rongeur, straight, 4" (100 mm), fenestrated, shaft in cm graduated, width: 6,50 mm

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
33442 Craniofacial rongeur, reusable

Identifiers

Type ID
Primary 04038653209538

Customer Contacts