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Disc Prep

FDA UDI

Class I (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Disc Prep FDA UDI
Generic Name
Bone graft funnel FDA UDI
Device Name
Funnel-Bone FDA UDI
Model / Reference
06-35-0825 FDA UDI
Description
Funnel-Bone FDA UDI

Identifiers

Catalog Number
06-35-0825 FDA UDI
Primary DI / UDI-DI
10889981103224 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone graft funnel 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone graft funnel

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

Similar devices

Also classified as Bone graft funnel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SeaSpine Orthopedics Corporation

Sources (1)

  • FDA UDI 4e70d1e4-153e-4e82-bb60-bb50c2cd6992 35 fields · synced Jun 8, 2026