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Sm

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
SM FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
Skin Stapler Reload FDA UDI
Model / Reference
050284 FDA UDI
Description
Skin Stapler Reload FDA UDI

Identifiers

Primary DI / UDI-DI
10884521080737 FDA UDI
FDA Product Code
GDT FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4760 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Sm by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 78f42092-98d7-41b5-8aa4-10c0a2fdcb94 37 fields · synced Jun 8, 2026