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H.a.s.®

FDA UDI

Class II (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
H.A.S.® FDA UDI
Generic Name
Whole-blood-recovery autotransfusion system, manual FDA UDI
Model / Reference
00-2555-060-05 FDA UDI

Identifiers

Primary DI / UDI-DI
00889024021600 FDA UDI
510(k) Number
K920273 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Whole-blood-recovery autotransfusion system, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Whole-blood-recovery autotransfusion system, manual

H.a.s.® by Zimmer Orthopaedic Surgical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Whole-blood-recovery autotransfusion system, manual.

Cleared under the same submission

K920273 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Orthopaedic Surgical Products

Sources (1)

  • FDA UDI df855351-75c0-4243-b7d4-7b0e7b21b09e 34 fields · synced May 30, 2026