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Forceps- Paper

FDA UDI

Class I (US FDA UDI)

by Whip-Mix Corp.

Identity

Trade Name
Forceps- Paper FDA UDI
Generic Name
Dental articulation paper forceps FDA UDI
Device Name
Forceps, Articulation Paper FDA UDI
Model / Reference
60300 FDA UDI
Description
Forceps, Articulation Paper FDA UDI

Identifiers

Primary DI / UDI-DI
D040603000 FDA UDI
FDA Product Code
EFK FDA UDI
GMDN Term
Dental articulation paper forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Dental articulation paper forceps

Forceps- Paper by Whip-Mix Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental articulation paper forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Whip-Mix Corp.

Sources (1)

  • FDA UDI 59e97f2b-0fb2-4b88-a261-507b462025de 33 fields · synced May 30, 2026