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Appui-Tete Reglable Amovible/ Adjustable Headrest

FDA UDI

Class II (US FDA UDI)

by Sarl Vipamat

Identity

Trade Name
APPUI-TETE REGLABLE AMOVIBLE/ ADJUSTABLE HEADREST FDA UDI
Generic Name
Wheelchair/chair/stander headrest FDA UDI
Model / Reference
0008-00-05 FDA UDI

Identifiers

Primary DI / UDI-DI
03664560000176 FDA UDI
510(k) Number
K051709 FDA UDI
FDA Product Code
IQC FDA UDI
GMDN Term
Wheelchair/chair/stander headrest FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3880 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair/chair/stander headrest

Appui-Tete Reglable Amovible/ Adjustable Headrest by Sarl Vipamat — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair/chair/stander headrest.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sarl Vipamat

Sources (1)

  • FDA UDI 5c2f8bd3-d53e-4121-947e-fbe565ef2366 33 fields · synced Jun 1, 2026