FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653076598 · Model: GF950C · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653076598
Version / Model
GF950C
Catalog Number
GF950C
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not 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
887882a0-ff86-4a44-a7d3-af42bd3c85a4
Distribution End Date
2018-11-10

Device Description

HAND VALVE W/CONNECTION HOSE 200MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
32596 Foetal vacuum extraction system cup, reusable

Identifiers

Type ID
Primary 04038653076598

Customer Contacts