FDA UDI In Commercial Distribution 🇺🇸 United States

S-Monovette®

DI: 04038917134521 · Model: 04.1932.001 · Sarstedt Aktiengesellschaft & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
S-Monovette®
Primary DI
04038917134521
Version / Model
04.1932.001
Catalog Number
04.1932.001
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
d9532a5b-9b49-43c8-9f06-2a155e3dee1c

Device Description

S-Monovette® 4.9ml K2E-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
No
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
PJE Blood/Plasma Collection Device For Dna Testing

GMDN Terms

Code Name
47587 Evacuated blood collection tube IVD, anticoagulant/separator

Identifiers

Type ID
Package 04038917028868
Primary 04038917134521
Unit of Use 04038917207133

Customer Contacts