← Back to catalogue

Shuttle Series B - Standard

FDA UDI

Class I (US FDA UDI)

by Sizewise Rentals, L.l.c.

Identity

Trade Name
Shuttle Series B - Standard FDA UDI
Generic Name
Mobile bariatric examination/treatment chair, electric FDA UDI
Device Name
120V Shuttle Series B 32" - LTC FDA UDI
Model / Reference
T1000-ST FDA UDI
Description
120V Shuttle Series B 32" - LTC FDA UDI

Identifiers

Primary DI / UDI-DI
00845699001064 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Mobile bariatric examination/treatment chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile bariatric examination/treatment chair, electric

Shuttle Series B - Standard by Sizewise Rentals, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile bariatric examination/treatment chair, electric.

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 3379d445-eccb-4aa1-9458-b5e04305858b 33 fields · synced Jun 6, 2026