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Biopsy Forceps

FDA UDI

Class II (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name
Biopsy Forceps FDA UDI
Generic Name
Endomyocardial biopsy forceps, single-use FDA UDI
Device Name
BIOPSY FORCEPS 5.5F STD 104CM FDA UDI
Model / Reference
504300 FDA UDI
Description
BIOPSY FORCEPS 5.5F STD 104CM FDA UDI

Identifiers

Catalog Number
504300 FDA UDI
Primary DI / UDI-DI
10705032056090 FDA UDI
510(k) Number
K810849 FDA UDI
FDA Product Code
DWZ FDA UDI
GMDN Term
Endomyocardial biopsy forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endomyocardial biopsy forceps, single-use

Biopsy Forceps by Cordis US Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endomyocardial biopsy forceps, single-use.

Cleared under the same submission

K810849 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis US Corp.

Sources (1)

  • FDA UDI 664f96f9-91a8-4cb4-8b96-8ecee8ac38dd 35 fields · synced Jun 1, 2026