FDA UDI In Commercial Distribution 🇺🇸 United States

TL 1000 Preinstallation set

DI: 00887761968370 · Model: 4058051 · Baxter Medical Systems GmbH + Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TL 1000 Preinstallation set
Primary DI
00887761968370
Version / Model
4058051
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
2022-12-15
Public Version
2
Public Version Date
2023-02-09
Public Version Status
Update
Public Device Record Key
0e6223e2-7005-4bff-89af-db41e1880379

Device Description

TruLight 1000 preinstallation set

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
KZF Device, medical examination, ac powered

GMDN Terms

Code Name
35954 Medical device service rail

Identifiers

Type ID
Primary 00887761968370

Customer Contacts

Phone
+4936715860