FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653335015 · Model: RT093R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653335015
Version / Model
RT093R
Catalog Number
RT093R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-19
Public Version
6
Public Version Date
2021-05-07
Public Version Status
Update
Public Device Record Key
b60e507a-3fcd-4a8b-a396-d698742a4b9b
Distribution End Date
2018-11-03

Device Description

ENDOSCOPE HOLD.W/BALL HINGE D:5/110MM

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
No
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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
35967 Surgical retraction system mounting frame, reusable

Identifiers

Type ID
Primary 04038653335015

Customer Contacts