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Lifestart

FDA UDI

Class II (US FDA UDI)

by Inspiration Healthcare Group Plc

Identity

Trade Name
Lifestart FDA UDI
Generic Name
Instrument/equipment drape, reusable, sterile FDA UDI
Device Name
LSA106 LifeStart Drape (single unit) FDA UDI
Model / Reference
LSA106 FDA UDI
Description
LSA106 LifeStart Drape (single unit) FDA UDI

Identifiers

Primary DI / UDI-DI
05060195340706 FDA UDI
FDA Product Code
MMP FDA UDI
GMDN Term
Instrument/equipment drape, reusable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Instrument/equipment drape, reusable, sterile

Lifestart by Inspiration Healthcare Group Plc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, reusable, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inspiration Healthcare Group Plc

Sources (1)

  • FDA UDI 14163949-0b0b-4d16-a3f1-8751171f13ad 34 fields · synced Jun 8, 2026