Identity
- Trade Name
- E-sphyg™ FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Device Name
- Connector-8002, FDA UDI
- Model / Reference
- 8002-2 FDA UDI
- Description
- Connector-8002, FDA UDI
Identifiers
- Catalog Number
- 8002-2 FDA UDI
- Primary DI / UDI-DI
- 00634782056452 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
Yes
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
No
FDA UDI
Category: Aneroid manual sphygmomanometer
E-sphyg™ by American Diagnostic Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Aneroid manual sphygmomanometer.
- e-mega® black, disinfectable one-piece cuff, small adult size 2-tube — Rudolf Riester GmbH & Co. KG · Class II
- BAUM — W.A. BAUM CO., INC. · Class II
- Amico Diagnostic Station — Amico Diagnostic Incorporated · Class II
- MDF® — MDF Instruments Medifriend Inc. · Class II
- DIXIEEMS — Wenzhou Caretek Medical Device Co., Ltd. · Class II
- Hopkins Medical Products® — HOPKINS UNIFORM COMPANY · Class II
- HEINE GAMMA® GP — Heine Optotechnik GmbH & Co. KG · Class II
- Aneroids (82 etc.) — Rashman Corp. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- American Diagnostic Corporation
Sources (1)
- FDA UDI 2f44169f-4cc6-4e3e-9a14-808827d48e78 35 fields · synced May 30, 2026