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Staplizer

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
STAPLIZER FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
13mm STAPLE CARRIER FDA UDI
Model / Reference
T113 FDA UDI
Description
13mm STAPLE CARRIER FDA UDI

Identifiers

Catalog Number
T113 FDA UDI
Primary DI / UDI-DI
10845854031735 FDA UDI
510(k) Number
K840566 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Cleared under the same submission

K840566 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 5b82c9ce-9a15-4532-a7e7-e6d5391d350a 38 fields · synced Jun 1, 2026