FDA UDI In Commercial Distribution 🇺🇸 United States

Pre-Install Set Helux Pro

DI: 00887761976450 · Model: 4108051 · Baxter Medical Systems GmbH + Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pre-Install Set Helux Pro
Primary DI
00887761976450
Version / Model
4108051
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
2023-03-07
Public Version
1
Public Version Date
2023-03-15
Public Version Status
New
Public Device Record Key
9909eb38-46b6-477e-aa42-c538e8fa38bc

Device Description

Pre-Install Set Helux Pro

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
FQP Lamp, operating-room

GMDN Terms

Code Name
35954 Medical device service rail

Identifiers

Type ID
Primary 00887761976450

Customer Contacts

Phone
+4936715860