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Pmt Corporation

FDA UDI

Class II (US FDA UDI)

by Pmt Corp.

Identity

Trade Name
PMT CORPORATION FDA UDI
Generic Name
Analytical scalp lead FDA UDI
Device Name
INTERCONNECTION CABLE, 5 CONTACT (5X1), MINI CONNECTOR, NON-STERILE FDA UDI
Model / Reference
2120-05-01B-NS FDA UDI
Description
INTERCONNECTION CABLE, 5 CONTACT (5X1), MINI CONNECTOR, NON-STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00650551025450 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Analytical scalp lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Analytical scalp lead

Pmt Corporation by Pmt Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pmt Corp.

Sources (1)

  • FDA UDI e5ce48df-4765-457a-93c0-52160357ddde 33 fields · synced May 30, 2026