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SteriTatt

FDA UDI

Class I (US FDA UDI)

by Flow X-Ray Corp.

Identity

Trade Name
SteriTatt FDA UDI
Generic Name
Tattoo ink, dermal FDA UDI
Device Name
25 Single Service SteriTatt Markers and 25 sterile needles FDA UDI
Model / Reference
90002 FDA UDI
Description
25 Single Service SteriTatt Markers and 25 sterile needles FDA UDI

Identifiers

Primary DI / UDI-DI
00843696195014 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Tattoo ink, dermal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tattoo ink, dermal

SteriTatt by Flow X-Ray Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tattoo ink, dermal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flow X-Ray Corp.

Sources (1)

  • FDA UDI 78d3db36-0d06-4852-b484-ac5c5c271864 34 fields · synced Jun 6, 2026