← Back to catalogue

Bard® Platinum Class™ Non-Retracting Grasping Forceps

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Platinum Class™ Non-Retracting Grasping Forceps FDA UDI
Generic Name
Flexible endoscopic stone-retrieval forceps, single-use FDA UDI
Device Name
Bard® Platinum Class™ Non-Retracting Grasping Forceps FDA UDI
Model / Reference
039690 FDA UDI
Description
Bard® Platinum Class™ Non-Retracting Grasping Forceps FDA UDI

Identifiers

Catalog Number
039690 FDA UDI
Primary DI / UDI-DI
00801741076558 FDA UDI
FDA Product Code
FFL FDA UDI
GMDN Term
Flexible endoscopic stone-retrieval forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4680 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 11 Millimeter FDA UDI
Length — 90 Centimeter FDA UDI

Category: Flexible endoscopic stone-retrieval forceps, single-use

Bard® Platinum Class™ Non-Retracting Grasping Forceps by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic stone-retrieval forceps, single-use.

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
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 99dfb261-80c7-4a6b-ad42-9ac01b9e3811 36 fields · synced May 31, 2026