FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653177806 · Model: OK900 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653177806
Version / Model
OK900
Catalog Number
OK900
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
ea8a2bf6-b4e5-4843-82f8-903077ce367e

Device Description

HAJEK Irrigation Cannula, straight, 6 1/2", (165 mm), diam. 3,50 mm, silver, luer hub, 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
Yes
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
GCX APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 04038653177806

Customer Contacts