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K.T.Surgico

FDA UDI

Class I (US FDA UDI)

by K.t.surgico

Identity

Trade Name
K.T.Surgico FDA UDI
Generic Name
General-purpose surgical scissors, single-use FDA UDI
Device Name
Mayo Scissor 6.75" CVD FDA UDI
Model / Reference
2025 FDA UDI
Description
Mayo Scissor 6.75" CVD FDA UDI

Identifiers

Catalog Number
KTS0816117 FDA UDI
Primary DI / UDI-DI
KTS0816117 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

K.T.Surgico by K.t.surgico — 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
K.t.surgico

Sources (1)

  • FDA UDI cb5351e0-60a2-498e-806b-23994b39832c 35 fields · synced Jun 8, 2026