← Back to catalogue

Glucagon - RIA

FDA UDI

Class I (US FDA UDI)

by Diasource Immunoassays, S.A.

Identity

Trade Name
Glucagon - RIA FDA UDI
Generic Name
Glucagon IVD, kit, enzyme immunohistochemistry FDA UDI
Device Name
Glucagon - RIA FDA UDI
Model / Reference
RB310 FDA UDI
Description
Glucagon - RIA FDA UDI

Identifiers

Primary DI / UDI-DI
05400569003019 FDA UDI
FDA Product Code
JME FDA UDI
GMDN Term
Glucagon IVD, kit, enzyme immunohistochemistry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1335 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucagon IVD, kit, enzyme immunohistochemistry

Glucagon - RIA by Diasource Immunoassays, S.A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 c1c3c827-be37-48e1-beb0-a87c4b1bed6a 33 fields · synced Jun 8, 2026