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Taylor Stitcher Punch

FDA UDI

Class I (US FDA UDI)

by Ncs Lab Srl

Identity

Trade Name
Taylor Stitcher Punch FDA UDI
Generic Name
Bone awl, reusable FDA UDI
Device Name
Surgical instrument to be used with Superelastic Transosseous Needle (STN). FDA UDI
Model / Reference
P005_AS034_03 FDA UDI
Description
Surgical instrument to be used with Superelastic Transosseous Needle (STN). FDA UDI

Identifiers

Primary DI / UDI-DI
08051122041145 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone awl, reusable 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

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: Bone awl, reusable

Taylor Stitcher Punch by Ncs Lab Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone awl, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ncs Lab Srl

Sources (1)

  • FDA UDI 799539f4-1298-48ea-a508-1da2c9295dba 33 fields · synced Jun 8, 2026