STA Satellite®

FDA UDI

Class II (US FDA UDI)

by Diagnostica Stago, Inc.

Identity

Trade Name: STA Satellite® FDA UDI
Generic Name: Coagulation analyser IVD, laboratory FDA UDI
Model / Reference: 58104 FDA UDI

Identifiers

Primary DI / UDI-DI: 03607450581041 FDA UDI
510(k) Number: K082248 FDA UDI
FDA Product Code: JPA FDA UDI
GMDN Term: Coagulation analyser IVD, laboratory FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 864.5425 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Coagulation analyser IVD, laboratory

STA Satellite® by Diagnostica Stago, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Diagnostica Stago, Inc.

Sources (1)

FDA UDI 9449a7e5-6de9-4029-899b-c844c0166d14 33 fields · synced Jun 7, 2026