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PowerCel™ 170 Mini

FDA UDI

Class III (US FDA UDI)

by Advanced Bionics

Identity

Trade Name
PowerCel™ 170 Mini FDA UDI
Generic Name
Secondary battery FDA UDI
Device Name
Carribean Pirate FDA UDI
Model / Reference
CI-5527-190 FDA UDI
Description
Carribean Pirate FDA UDI

Identifiers

Primary DI / UDI-DI
00840094448476 FDA UDI
PMA Number
P960058 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Secondary battery FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Secondary battery

PowerCel™ 170 Mini by Advanced Bionics — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secondary battery.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Bionics

Sources (1)

  • FDA UDI b9a4c24d-987d-4f54-8c32-01340691b3e2 36 fields · synced Jun 1, 2026