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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MD Atlas
M.D.L. S.r.l.

Data from EUDAMED, last updated May 31, 2026

VeressA

B-08032986351021

1 reference

Class IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Risk category: Class IIa
Manufacturer: M.D.L. S.r.l.

Device family identification

Device name: VeressA
Basic UDI-DI: B-08032986351021
Device model: AVA1610
Issuing agency: EUDAMED
Version date: Feb 24, 2026

Classification

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Risk category: Class IIa
Status: On the market

Manufacturer

Manufacturer

Name: M.D.L. S.r.l.
SRN: IT-MF-000011599
Country: Italy
Email: info@mdlsrl.com
Phone: +39 0342 682130

Device characteristics

No device characteristics flagged

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

K0104Veress needles

References by status

Legacy certificates

Certificate number: 166-02-03-DM
Type: refdata.legacy.mdd-certificate-type.v
Notified body: ITALCERT SRL (0426)
Validity: Dec 19, 2023

References

1 reference

Export results

Applied filters

basicUdiUlid01KJ7XA176BRK5YWV8QBH08Y88

Format

Summary

31 columns included

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
AVA1610	`AVA1610`	`08032986351021`	1	On the market