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Delacroix-Chevalier

FDA UDI

Class I (US FDA UDI)

by Landanger

Identity

Trade Name
DELACROIX-CHEVALIER FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Model / Reference
DC83211-36 FDA UDI

Identifiers

Primary DI / UDI-DI
03661219320258 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

Delacroix-Chevalier by Landanger — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Landanger

Sources (1)

  • FDA UDI ed89c8de-4902-4f17-a63a-4c3d4a373d39 32 fields · synced Jun 8, 2026