← Back to catalogue

Instrument For Angulation Of Distal Angled Implants. Double Ended

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
INSTRUMENT FOR ANGULATION OF DISTAL ANGLED IMPLANTS. DOUBLE ENDED FDA UDI
Generic Name
General-purpose calliper, metallic FDA UDI
Model / Reference
10-8076HD FDA UDI

Identifiers

Primary DI / UDI-DI
D928108076HD0 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
General-purpose calliper, metallic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose calliper, metallic

Instrument For Angulation Of Distal Angled Implants. Double Ended by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose calliper, metallic.

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
W.H. Holden, Inc.

Sources (1)

  • FDA UDI 303b5c6e-bee5-4a24-9822-6a2028696aa5 32 fields · synced May 30, 2026