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Sklar

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar FDA UDI
Generic Name
Abdominal/intestinal spatula FDA UDI
Device Name
TURNER WARWICK AB SPAT114X57MM FDA UDI
Model / Reference
60-7424 FDA UDI
Description
TURNER WARWICK AB SPAT114X57MM FDA UDI

Identifiers

Primary DI / UDI-DI
10649111454363 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Abdominal/intestinal spatula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Abdominal/intestinal spatula

Sklar by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal/intestinal spatula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI d63d95cb-bd59-483a-955f-b3d7cad8346a 33 fields · synced Jun 8, 2026