← Back to catalogue

LITe DECOMPRESSION

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
LITe DECOMPRESSION FDA UDI
Generic Name
Lumbar interspinous decompression instrument set, reusable FDA UDI
Device Name
TUBE FDA UDI
Model / Reference
48081604 FDA UDI
Description
TUBE FDA UDI

Identifiers

Catalog Number
48081604 FDA UDI
Primary DI / UDI-DI
07613327264074 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Lumbar interspinous decompression instrument set, 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 4.0 Centimeter FDA UDI

Category: Lumbar interspinous decompression instrument set, reusable

LITe DECOMPRESSION by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumbar interspinous decompression instrument set, 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
Stryker Corp.

Sources (1)

  • FDA UDI 588ef132-8988-4e69-9385-88014cebf668 35 fields · synced Jun 8, 2026