← Back to catalogue

Velnez

FDA UDI

Class I (US FDA UDI)

by Datt Mediproducts Private Limited

Identity

Trade Name
Velnez FDA UDI
Generic Name
Intranasal splint, non-bioabsorbable, animal-derived FDA UDI
Device Name
VELNEZ Nasal Pack 10 cm x 2 cm FDA UDI
Model / Reference
141002-05 FDA UDI
Description
VELNEZ Nasal Pack 10 cm x 2 cm FDA UDI

Identifiers

Primary DI / UDI-DI
08904340408163 FDA UDI
FDA Product Code
LYA FDA UDI
GMDN Term
Intranasal splint, non-bioabsorbable, animal-derived FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4780 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 10 Centimeter FDA UDI
Width — 2 Centimeter FDA UDI

Category: Intranasal splint, non-bioabsorbable, animal-derived

Velnez by Datt Mediproducts Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-bioabsorbable, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1d4ead1b-f867-4d6d-8824-bdd35a41ba20 36 fields · synced Jun 1, 2026