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Buffalo Dental Mfg

FDA UDI

Class I (US FDA UDI)

by Buffalo Dental Manufacturing Co., Inc.

Identity

Trade Name
Buffalo Dental Mfg FDA UDI
Generic Name
Dental dressing forceps, reusable FDA UDI
Device Name
Tweezer 175A curved FDA UDI
Model / Reference
83740 FDA UDI
Description
Tweezer 175A curved FDA UDI

Identifiers

Catalog Number
83740 FDA UDI
Primary DI / UDI-DI
00850043381280 FDA UDI
FDA Product Code
EFL FDA UDI
GMDN Term
Dental dressing forceps, reusable 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

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

No

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: Dental dressing forceps, reusable

Buffalo Dental Mfg by Buffalo Dental Manufacturing Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental dressing forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6813bde4-23c5-4768-94d9-c77a95ff3d40 34 fields · synced May 30, 2026