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Digitex

FDA UDI

Class I (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Digitex FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
Suture Delivery Device FDA UDI
Model / Reference
52025 FDA UDI
Description
Suture Delivery Device FDA UDI

Identifiers

Catalog Number
52025 FDA UDI
Primary DI / UDI-DI
05708932440127 FDA UDI
510(k) Number
K093112 FDA UDI
FDA Product Code
HCF FDA UDI
GMDN Term
Suturing unit, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suturing unit, single-use

Digitex by Coloplast A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Cleared under the same submission

K093112 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI b252c5aa-745c-4997-9cda-dc68c9cca74d 37 fields · synced May 30, 2026