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Caplock

FDA UDI

Class I (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
Caplock FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
Caplock - Capsular Passer 70° FDA UDI
Model / Reference
Capsular Passer 70° FDA UDI
Description
Caplock - Capsular Passer 70° FDA UDI

Identifiers

Catalog Number
361-70 FDA UDI
Primary DI / UDI-DI
07899258662633 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Suturing unit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suturing unit, single-use

Caplock by Gm Dos Reis Industria E Comercio Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2da80cfc-dd95-455e-8a80-4f7d31a00518 34 fields · synced May 31, 2026