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Caretaker4

FDA UDI

Class II (US FDA UDI)

by Caretaker Medical, LLC

Identity

Trade Name
Caretaker4 FDA UDI
Generic Name
Cosmetic micro-needling manual roller/stamp, reusable FDA UDI
Device Name
Wireless Vital Signs Monitor FDA UDI
Model / Reference
CT4 FDA UDI
Description
Wireless Vital Signs Monitor FDA UDI

Identifiers

Catalog Number
CT4 FDA UDI
Primary DI / UDI-DI
00864609000300 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Cosmetic micro-needling manual roller/stamp, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cosmetic micro-needling manual roller/stamp, reusable

Caretaker4 by Caretaker Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a6506b1-6219-49e0-b065-3d0f41bf1dde 36 fields · synced Jun 8, 2026