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Anterior Disc Prep

FDA UDI

Class I (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Anterior Disc Prep FDA UDI
Generic Name
Scalpel handle, reusable FDA UDI
Device Name
Scalpel Handle #3 12 inch FDA UDI
Model / Reference
95-6989 FDA UDI
Description
Scalpel Handle #3 12 inch FDA UDI

Identifiers

Catalog Number
95-6989 FDA UDI
Primary DI / UDI-DI
10889981184537 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Scalpel handle, 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: Scalpel handle, 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 Scalpel handle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96aa0d8a-f0fc-4229-858e-2046b5a3b289 35 fields · synced Jun 8, 2026