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Aft

FDA UDI

Class I (US FDA UDI)

by Hill Laboratories

Identity

Trade Name
AFT FDA UDI
Generic Name
Body arch traction table FDA UDI
Model / Reference
AFT FDA UDI

Identifiers

Primary DI / UDI-DI
00860011173618 FDA UDI
FDA Product Code
HST FDA UDI
GMDN Term
Body arch traction table FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Body arch traction table

Aft by Hill Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body arch traction table.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hill Laboratories

Sources (1)

  • FDA UDI 4b329fda-72bf-4a03-a5d2-c95b6fe55e79 32 fields · synced May 30, 2026