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Castroviejo Suturing Forceps (1.2 mm)

FDA UDI

Class I (US FDA UDI)

by Oculo-Plastik Inc

Identity

Trade Name
Castroviejo Suturing Forceps (1.2 mm) FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Device Name
Stainless Steel Suturing Forceps (non glare) FDA UDI
Model / Reference
25-112 FDA UDI
Description
Stainless Steel Suturing Forceps (non glare) FDA UDI

Identifiers

Primary DI / UDI-DI
10697660003495 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 1.2 Millimeter FDA UDI
Length — 10 Centimeter FDA UDI

Castroviejo Suturing Forceps (1.2 mm) by Oculo-Plastik Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oculo-Plastik Inc

Sources (1)

  • FDA UDI 74b4f7d7-1fba-4735-9215-a7e124d1a38e 36 fields · synced Jun 1, 2026