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BE-ST NIM PAK Needle Trocar

FDA UDI

Class II (US FDA UDI)

by Lacey Manufacturing Company Llc

Identity

Trade Name
BE-ST NIM PAK Needle Trocar FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
Pedicle Access Kit Needle with Neural Integrity Monitor FDA UDI
Model / Reference
PK1007 FDA UDI
Description
Pedicle Access Kit Needle with Neural Integrity Monitor FDA UDI

Identifiers

Catalog Number
PK1007 FDA UDI
Primary DI / UDI-DI
00853508002287 FDA UDI
FDA Product Code
PDQ FDA UDI
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10.95 Inch FDA UDI

Category: Bone access cannula

BE-ST NIM PAK Needle Trocar by Lacey Manufacturing Company Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b8fc6b79-9eb3-46cb-8a6f-fb6e38c459d1 36 fields · synced May 30, 2026