← Back to catalogue

Iodine Qc Level 2

FDA UDI

Class I (US FDA UDI)

by Utak Laboratories, Inc.

Identity

Trade Name
IODINE QC LEVEL 2 FDA UDI
Generic Name
Multiple-type clinical chemistry analyte profile IVD, control FDA UDI
Device Name
IODINE QC LEVEL 2 FDA UDI
Model / Reference
IOD QC 2 U QDVA FDA UDI
Description
IODINE QC LEVEL 2 FDA UDI

Identifiers

Catalog Number
IOD QC 2 U QDVA FDA UDI
Primary DI / UDI-DI
B800IODQC2UQDVA0 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Multiple-type clinical chemistry analyte profile IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Category: Multiple-type clinical chemistry analyte profile IVD, control

Iodine Qc Level 2 by Utak Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type clinical chemistry analyte profile IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 179c4d31-ca78-49e1-9916-9e8a5bf7f68c 37 fields · synced Jun 8, 2026