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Conmed

FDA UDI

Class III (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Pin-indexed adaptor, reusable FDA UDI
Device Name
Multifunction Electrode Test Component FDA UDI
Model / Reference
SHRTG BLOCK FDA UDI
Description
Multifunction Electrode Test Component FDA UDI

Identifiers

Catalog Number
SHRTG BLOCK FDA UDI
Primary DI / UDI-DI
10653405046813 FDA UDI
510(k) Number
K003548 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Pin-indexed adaptor, reusable FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pin-indexed adaptor, reusable

Conmed by Conmed Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin-indexed adaptor, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 07b348ad-ec88-420e-829d-1421ddd0d818 37 fields · synced May 30, 2026