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Amvia Sky HF-T

FDA UDI

Class III (US FDA UDI)

by BIOTRONIK SE & Co. KG

Identity

Trade Name
Amvia Sky HF-T FDA UDI
Generic Name
Cardiac resynchronization therapy implantable pacemaker FDA UDI
Model / Reference
460159 FDA UDI

Identifiers

Catalog Number
460159 FDA UDI
Primary DI / UDI-DI
04035479174033 FDA UDI
PMA Number
P950037 FDA UDI
FDA Product Code
NKE FDA UDI
GMDN Term
Cardiac resynchronization therapy implantable pacemaker 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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cardiac resynchronization therapy implantable pacemaker

Amvia Sky HF-T by BIOTRONIK SE & Co. KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac resynchronization therapy implantable pacemaker.

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 7f9bc148-eb72-4c05-a9c9-5846f75d4e2d 36 fields · synced Jun 8, 2026