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1% KCl GEL

FDA UDI

Class II (US FDA UDI)

by Parker Laboratories, Inc.

Identity

Trade Name
1% KCl GEL FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
Bulk packed 1% KCl gel FDA UDI
Model / Reference
99-01-730090 FDA UDI
Description
Bulk packed 1% KCl gel FDA UDI

Identifiers

Catalog Number
99-01-730090 FDA UDI
Primary DI / UDI-DI
00855683006920 FDA UDI
FDA Product Code
GYB FDA UDI
GMDN Term
Electrode conductive medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1275 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

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: Electrode conductive medium

1% KCl GEL by Parker Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b6ddeeaf-dc62-4612-9196-9725ae7133ba 35 fields · synced Jun 8, 2026