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Lattus

FDA UDI

Class I (US FDA UDI)

by Tedan Surgical Innovations, L.l.c.

Identity

Trade Name
Lattus FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
CENTER BLADE, 100 MM, SST FDA UDI
Model / Reference
LAT-0831 FDA UDI
Description
CENTER BLADE, 100 MM, SST FDA UDI

Identifiers

Primary DI / UDI-DI
00843059124798 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Category: Surgical retractor/retraction system blade, reusable

Lattus by Tedan Surgical Innovations, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tedan Surgical Innovations, L.l.c.

Sources (1)

  • FDA UDI 3635aadd-9062-479e-b3f0-f73dafa98dcb 33 fields · synced Jun 1, 2026