FDA UDI In Commercial Distribution 🇺🇸 United States

Minivette® POCT 50µl LH, US

DI: 04038917320023 · Model: 17.2112.150 · Sarstedt Aktiengesellschaft & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
Minivette® POCT 50µl LH, US
Primary DI
04038917320023
Version / Model
17.2112.150
Catalog Number
17.2112.150
Company Name
Sarstedt Aktiengesellschaft & Co.KG
Labeler DUNS
388000270
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2022-11-30
Public Version
1
Public Version Date
2022-12-08
Public Version Status
New
Public Device Record Key
9967a739-3b3e-4d42-a713-0c3e0152e52d

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
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GIO TUBE, COLLECTION, CAPILLARY BLOOD

GMDN Terms

Code Name
61388 Capillary blood collection tube IVD, lithium heparin

Identifiers

Type ID
Unit of Use 04038917320030
Primary 04038917320023

Customer Contacts