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Scissors

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
SCISSORS FDA UDI
Generic Name
Neurosurgical scissors FDA UDI
Device Name
TEW, STRAIGHT, SERRATED, 2.5 MM BLADES FDA UDI
Model / Reference
07-002-80-07 FDA UDI
Description
TEW, STRAIGHT, SERRATED, 2.5 MM BLADES FDA UDI

Identifiers

Primary DI / UDI-DI
00888118009593 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
Neurosurgical scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical scissors

Scissors by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI 43896bc2-d630-423b-9399-c1c24e41b472 34 fields · synced Jun 8, 2026