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Diamatrix

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix FDA UDI
Generic Name
Ocular hook/spatula/manipulator, reusable FDA UDI
Device Name
Castroviejo Caliper, Straight shaft, 0-20mm measuring scale visable from both sides, Fine threaded control screw for maintaining consistent control, Stainless Steel FDA UDI
Model / Reference
M70S-C FDA UDI
Description
Castroviejo Caliper, Straight shaft, 0-20mm measuring scale visable from both sides, Fine threaded control screw for maintaining consistent control, Stainless Steel FDA UDI

Identifiers

Catalog Number
M70S-C FDA UDI
Primary DI / UDI-DI
00813059016089 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Ocular hook/spatula/manipulator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ocular hook/spatula/manipulator, reusable

Diamatrix by Diamatrix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ocular hook/spatula/manipulator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI 9f3716ab-f0b2-45ea-88ec-7455b5351de4 34 fields · synced May 30, 2026