← Back to catalogue

Restylane 0.5 ML.+ Lidocaine

FDA UDI

Class III (US FDA UDI)

by Lambsmead Ltd

Identity

Trade Name
Restylane 0.5 ML.+ Lidocaine FDA UDI
Generic Name
Dermal tissue reconstructive material, microbe-derived, anaesthetic FDA UDI
Model / Reference
170101 FDA UDI

Identifiers

Primary DI / UDI-DI
05060457760129 FDA UDI
FDA Product Code
LMH FDA UDI
GMDN Term
Dermal tissue reconstructive material, microbe-derived, anaesthetic 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, microbe-derived, anaesthetic

Restylane 0.5 ML.+ Lidocaine by Lambsmead Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermal tissue reconstructive material, microbe-derived, anaesthetic.

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

Manufacturer
Lambsmead Ltd

Sources (1)

  • FDA UDI 194f377a-18e4-4229-b272-16cb1c945763 32 fields · synced May 29, 2026