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JuiceBLOK, (Li-Ion) AC Power Bank

FDA UDI

Class I (US FDA UDI)

by Delfi Medical Innovations Inc

Identity

Trade Name
JuiceBLOK, (Li-Ion) AC Power Bank FDA UDI
Generic Name
Surgical pneumatic tourniquet system FDA UDI
Device Name
The JUICEBLOK is designed to be used with the PTS Roll Stand. Mountable to PTS Roll Stand in single and dual configurations. FDA UDI
Model / Reference
9-2200-600 FDA UDI
Description
The JUICEBLOK is designed to be used with the PTS Roll Stand. Mountable to PTS Roll Stand in single and dual configurations. FDA UDI

Identifiers

Primary DI / UDI-DI
M995922006001 FDA UDI
FDA Product Code
KCY FDA UDI
GMDN Term
Surgical pneumatic tourniquet system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 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

Yes

FDA UDI

Category: Surgical pneumatic tourniquet system

JuiceBLOK, (Li-Ion) AC Power Bank by Delfi Medical Innovations Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical pneumatic tourniquet system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f1de8ad-64db-43eb-a2f8-19ce8876972e 34 fields · synced May 30, 2026