FDA UDI In Commercial Distribution 🇺🇸 United States

VidiaPort

DI: 00887761968462 · Model: 4028210 · Baxter Medical Systems GmbH + Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VidiaPort
Primary DI
00887761968462
Version / Model
4028210
Company Name
Baxter Medical Systems GmbH + Co. KG
Labeler DUNS
330961223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-05
Public Version
2
Public Version Date
2023-02-09
Public Version Status
Update
Public Device Record Key
ca8adebc-f039-4900-b5b3-ea4ce0d37f75

Device Description

VidiaPort Ceiling Duo

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQM CAMERA, SURGICAL AND ACCESSORIES

GMDN Terms

Code Name
37332 Operating room light system

Identifiers

Type ID
Primary 00887761968462

Customer Contacts

Phone
+4936715860