Level One, Sterile

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name: LEVEL ONE, STERILE FDA UDI
Generic Name: Surgical screwdriver, single-use FDA UDI
Device Name: BLADE, SCREWDRIVER, ANGULUS II, MAXDRIVE, 1.5 MM FDA UDI
Model / Reference: 50-991-15-71 FDA UDI
Description: BLADE, SCREWDRIVER, ANGULUS II, MAXDRIVE, 1.5 MM FDA UDI

Identifiers

Primary DI / UDI-DI: 00888118096593 FDA UDI
FDA Product Code: HXX FDA UDI
GMDN Term: Surgical screwdriver, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical screwdriver, single-use

Level One, Sterile by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: KLS-Martin L.P.

Sources (1)

FDA UDI 071dd563-f9d4-4f14-b2f8-44b1cb4f460b 35 fields · synced Jun 8, 2026