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activL®

FDA UDI

Class III (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
activL® FDA UDI
Generic Name
Lumbar total intervertebral disc prosthesis FDA UDI
Device Name
ACTIV L PE-INLAY 14MM FDA UDI
Model / Reference
SW968 FDA UDI
Description
ACTIV L PE-INLAY 14MM FDA UDI

Identifiers

Catalog Number
SW968 FDA UDI
Primary DI / UDI-DI
04038653430970 FDA UDI
FDA Product Code
MJO FDA UDI
GMDN Term
Lumbar total intervertebral disc prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Lumbar total intervertebral disc prosthesis

activL® by Aesculap, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumbar total intervertebral disc prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI a80e102b-bfe7-47cb-948b-cfb7952e2b47 36 fields · synced May 30, 2026