FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653320547 · Model: PF010A · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653320547
Version / Model
PF010A
Catalog Number
PF010A
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-30
Public Version
8
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
02c3f986-56b6-421c-99f5-7d5bb44a21fa

Device Description

PAEDISCOPE FLEXIBLE SCOPE

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
Yes
Has Lot/Batch Number
No
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
GWG ENDOSCOPE, NEUROLOGICAL

GMDN Terms

Code Name
36904 Rigid optical intracranial/spinal endoscope, reusable

Identifiers

Type ID
Primary 04038653320547

Customer Contacts