← Back to catalogue

Tinto Glucagon

FDA UDI

Class I (US FDA UDI)

by Bio Sb, Inc.

Identity

Trade Name
Tinto Glucagon FDA UDI
Generic Name
Glucagon IVD, antibody FDA UDI
Device Name
Tinto Glucagon FDA UDI
Model / Reference
Predilute, 15 ml FDA UDI
Description
Tinto Glucagon FDA UDI

Identifiers

Catalog Number
BSB 5577 FDA UDI
Primary DI / UDI-DI
B502BSB55770 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Glucagon IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Glucagon IVD, antibody

Tinto Glucagon by Bio Sb, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucagon IVD, antibody.

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

Manufacturer
Bio Sb, Inc.

Sources (1)

  • FDA UDI aa0722db-6c6c-4b86-9ca8-229b25443aa9 34 fields · synced Jun 8, 2026