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FRU Ultra Lens Cover

FDA UDI

Class II (US FDA UDI)

by Accutron

Identity

Trade Name
FRU Ultra Lens Cover FDA UDI
Generic Name
Inhalational analgesia unit FDA UDI
Model / Reference
24551 FDA UDI

Identifiers

Catalog Number
24551 FDA UDI
Primary DI / UDI-DI
00813830020311 FDA UDI
510(k) Number
K970163 FDA UDI
FDA Product Code
BSZ FDA UDI
GMDN Term
Inhalational analgesia unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5160 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

FRU Ultra Lens Cover by Accutron — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accutron

Sources (1)

  • FDA UDI 0717885f-5057-4436-9111-592f1e6cb69d 35 fields · synced Jun 8, 2026