← Back to catalogue

Anchor Bolt Kit, LSB Style

FDA UDI

Class II (US FDA UDI)

by Ad-Tech Medical Instrument Corp.

Identity

Trade Name
Anchor Bolt Kit, LSB Style FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Model / Reference
LSBK1-AX-05 FDA UDI

Identifiers

Catalog Number
LSBK1-AX-05 FDA UDI
Primary DI / UDI-DI
00841823104267 FDA UDI
FDA Product Code
GZL FDA UDI
GMDN Term
Neurological stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1330 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neurological stereotactic surgery system

Anchor Bolt Kit, LSB Style by Ad-Tech Medical Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 79f70fed-d734-47a9-b4f0-000b260f2858 35 fields · synced Jun 9, 2026