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Reprocessed MicroNeedle 3cm

FDA UDI

Class II (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed MicroNeedle 3cm FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed FDA UDI
Model / Reference
138505-10 FDA UDI

Identifiers

Primary DI / UDI-DI
B390138505101 FDA UDI
FDA Product Code
NUJ FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

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: Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed

Reprocessed MicroNeedle 3cm by Suretek Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Suretek Medical

Sources (1)

  • FDA UDI deb2d6f0-3eac-44f3-a8e9-cff4c8c1468f 32 fields · synced May 30, 2026