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Accutray

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
ACCUTRAY FDA UDI
Generic Name
Epidural anaesthesia set, medicated FDA UDI
Model / Reference
5200208 FDA UDI

Identifiers

Primary DI / UDI-DI
10809160001691 FDA UDI
FDA Product Code
OFT FDA UDI
GMDN Term
Epidural anaesthesia set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Epidural anaesthesia set, medicated

Accutray by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epidural anaesthesia set, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02b1a9b3-8b43-4646-8cdb-2a7734082ea4 33 fields · synced Jun 8, 2026