← Back to catalogue

Wunder Rs300 Patient Scale Birdie Evo Xplus

FDA UDI

Class I (US FDA UDI)

by Invacare Corp.

Identity

Trade Name
WUNDER RS300 PATIENT SCALE BIRDIE EVO XPLUS FDA UDI
Generic Name
Patient sling scale FDA UDI
Device Name
WUNDER RS300 PATIENT SCALE BIRDIE EVO XPLUS FDA UDI
Model / Reference
BLS5 FDA UDI
Description
WUNDER RS300 PATIENT SCALE BIRDIE EVO XPLUS FDA UDI

Identifiers

Primary DI / UDI-DI
05600494138736 FDA UDI
FDA Product Code
FRW FDA UDI
GMDN Term
Patient sling scale FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient sling scale

Wunder Rs300 Patient Scale Birdie Evo Xplus by Invacare Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient sling scale.

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
Invacare Corp.

Sources (1)

  • FDA UDI 8e9a3815-4404-463e-9976-fef44fd7c1d4 34 fields · synced May 31, 2026