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Synermed®

FDA UDI

Class I (US FDA UDI)

by Infrared Laboratory Systems Llc

Identity

Trade Name
Synermed® FDA UDI
Generic Name
Unsaturated iron binding capacity (UIBC) IVD, reagent FDA UDI
Device Name
UIBC Binding Buffer Reagent 6 X 490 mL _ 6 X 10 mL FDA UDI
Model / Reference
IR151-L FDA UDI
Description
UIBC Binding Buffer Reagent 6 X 490 mL _ 6 X 10 mL FDA UDI

Identifiers

Catalog Number
IR151-L FDA UDI
Primary DI / UDI-DI
05060500091453 FDA UDI
510(k) Number
K922784 FDA UDI
FDA Product Code
JMO FDA UDI
GMDN Term
Unsaturated iron binding capacity (UIBC) IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1415 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Unsaturated iron binding capacity (UIBC) IVD, reagent

Synermed® by Infrared Laboratory Systems Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unsaturated iron binding capacity (UIBC) IVD, reagent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ca92f4d-6b4c-45f8-b103-a51d346bb155 37 fields · synced Jun 8, 2026