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Restylane Vital 1 ML.

FDA UDI

Class III (US FDA UDI)

by Lambsmead Ltd

Identity

Trade Name
Restylane Vital 1 ML. FDA UDI
Generic Name
Dermal tissue reconstructive material, animal-derived FDA UDI
Model / Reference
1070603 FDA UDI

Identifiers

Primary DI / UDI-DI
05060457760181 FDA UDI
FDA Product Code
LMH FDA UDI
GMDN Term
Dermal tissue reconstructive material, animal-derived FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dermal tissue reconstructive material, animal-derived

Restylane Vital 1 ML. by Lambsmead Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermal tissue reconstructive material, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lambsmead Ltd

Sources (1)

  • FDA UDI 1210afca-ea39-474d-a970-2fc93444b16c 32 fields · synced May 30, 2026