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Orsiro Mission

FDA UDI

Class III (US FDA UDI)

by Biotronik, Inc.

Identity

Trade Name
Orsiro Mission FDA UDI
Generic Name
Drug-eluting coronary artery stent, bioabsorbable-polymer-coated FDA UDI
Model / Reference
2.25/9/140 FDA UDI

Identifiers

Catalog Number
453925 FDA UDI
Primary DI / UDI-DI
07640130455818 FDA UDI
FDA Product Code
NIQ FDA UDI
GMDN Term
Drug-eluting coronary artery stent, bioabsorbable-polymer-coated FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Drug-eluting coronary artery stent, bioabsorbable-polymer-coated

Orsiro Mission by Biotronik, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Drug-eluting coronary artery stent, bioabsorbable-polymer-coated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotronik, Inc.

Sources (1)

  • FDA UDI b1a958a7-d39b-4c1e-b26f-810cef41bad3 36 fields · synced Jun 6, 2026