← Back to catalogue

Anterior Disc Prep

FDA UDI

Class I (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Anterior Disc Prep FDA UDI
Generic Name
Collection syringe adaptor, reusable FDA UDI
Device Name
ALIF Modular Distractor Tip - 8mm FDA UDI
Model / Reference
95-6192 FDA UDI
Description
ALIF Modular Distractor Tip - 8mm FDA UDI

Identifiers

Catalog Number
95-6192 FDA UDI
Primary DI / UDI-DI
10889981189327 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Collection syringe adaptor, 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: Collection syringe adaptor, reusable

Anterior Disc Prep by SeaSpine Orthopedics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collection syringe adaptor, reusable.

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

Manufacturer
SeaSpine Orthopedics Corporation

Sources (1)

  • FDA UDI fb9e6a4c-546a-4624-9ee1-57c043be8d28 35 fields · synced Jun 8, 2026