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Castroveijo Suturing Forcep 0.35

FDA UDIEUDAMED

Class I (US FDA UDI)

by Daud Jee Mfg. Co

Identity

Trade Name
CASTROVEIJO SUTURING FORCEP 0.35 FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
This instrument is used to grasp, retract, or stabilize tissue. FDA UDI
Model / Reference
D50-700011-2 FDA UDI
Description
This instrument is used to grasp, retract, or stabilize tissue. FDA UDI

Identifiers

Catalog Number
D50-700011-2 FDA UDI
Primary DI / UDI-DI
G006D5070001120 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, 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

Yes

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

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Castroveijo Suturing Forcep 0.35 by Daud Jee Mfg. Co — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Daud Jee Mfg. Co

Sources (2)

  • FDA UDI 65ad3f1a-234d-4696-bced-e473c8973c08 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026