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Intra-Lock

FDA UDI

Class I (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Intra-Lock FDA UDI
Generic Name
Dental rongeur FDA UDI
Device Name
Surgical Tissue Forceps FDA UDI
Model / Reference
BSTF FDA UDI
Description
Surgical Tissue Forceps FDA UDI

Identifiers

Catalog Number
BSTF FDA UDI
Primary DI / UDI-DI
D742BSTF0 FDA UDI
FDA Product Code
EMH FDA UDI
GMDN Term
Dental rongeur 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental rongeur

Intra-Lock by Intra-Lock International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca0e535f-e54c-4384-9279-1f9832e160fd 35 fields · synced Jun 8, 2026