FDA UDI In Commercial Distribution 🇺🇸 United States

Marketlab Inc

DI: 00817517020502 · Model: 5602 · MARKETLAB INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Marketlab Inc
Primary DI
00817517020502
Version / Model
5602
Catalog Number
5602
Company Name
MARKETLAB INC.
Labeler DUNS
848917027
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-11-16
Public Version
2
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
25ba3eb4-fcb6-4d14-b560-016c06b4938b

Device Description

Serum Capillary Collection-200ul 50/pk.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GIO TUBE, COLLECTION, CAPILLARY BLOOD

GMDN Terms

Code Name
35770 Capillary blood collection tube IVD, no additive

Identifiers

Type ID
Primary 00817517020502
Unit of Use 00817517021288

Customer Contacts