FDA UDI In Commercial Distribution 🇺🇸 United States

S-Monovette®

DI: 04038917134682 · Model: 04.1935.001 · Sarstedt Aktiengesellschaft & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
S-Monovette®
Primary DI
04038917134682
Version / Model
04.1935.001
Catalog Number
04.1935.001
Company Name
Sarstedt Aktiengesellschaft & Co.KG
Labeler DUNS
388000270
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
87680c63-6cd5-46b9-92ac-2fe428d3a4bf

Device Description

S-Monovette® 4.9ml Z-Gel

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
41128 Evacuated blood collection tube IVD, clot activator/separator

Identifiers

Type ID
Package 04038917025850
Primary 04038917134682
Unit of Use 04038917207256

Customer Contacts